Clinical Trials for Throat Disorders

Currently registered clinical trials for Throat Disorders from ClinicalTrials.gov. 18 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Throat Disorders from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 18
  • Active, not recruiting: 11
  • Completed: 9
  • Other: 12

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT02012699 — Integrated Cancer Repository for Cancer Research

StatusRecruiting
PhaseN/A
SponsorUniversity of Nebraska
Enrollment999999
Study TypeOBSERVATIONAL
ConditionsPancreatic Cancer; Thyroid Cancer; Lung Cancer; Esophageal Cancer; Thymus Cancer

The iCaRe2 is a multi-institutional resource created and maintained by the Fred & Pamela Buffett Cancer Center to collect and manage standardized, multi-dimensional, longitudinal data and biospecimens on consented adult cancer patients, high-risk individuals, and normal controls. The distinct characteristic of the iCaRe2 is its geographical coverage, with a significant percentage of small and …

NCT03093909 — Study of Aerosol Gemcitabine in Patients With Solid Tumors and Pulmonary Metastases

StatusRecruiting
PhasePhase 1
SponsorM.D. Anderson Cancer Center
Enrollment44
Study TypeINTERVENTIONAL
ConditionsMalignant Neoplasm of Bone and Articular Cartilage; Malignant Neoplasms of Female Genital Organs; Malignant Neoplasms of Independent (Primary) Multiple Sites; Malignant Neoplasms of Lip Oral Cavity and Pharynx; Malignant Neoplasm of Male Genital Organs
Interventions

Any time the words “you,” “your,” “I,” or “me” appear, it is meant to apply to the potential participant.

The goal of this clinical research study is to find the highest tolerable dose of gemcitabine that can be given by inhalation (breathing it as a mist) to patients with solid tumors that have spread to the lungs from other parts of the body.

The safety and side effects of this drug will al…

NCT04151082 — High Dose Steroid Therapy (Prednisone or Methylprednisolone) for the Improvement of Symptoms of Late Radiation-Associated Lower Cranial Neuropathy in Oropharyngeal Cancer Survivors

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorM.D. Anderson Cancer Center
Enrollment35
Study TypeINTERVENTIONAL
ConditionsCranial Nerve Disorder; Head and Neck Carcinoma; Oropharyngeal Carcinoma
Interventions; ;

This phase I/II trial studies the side effect and best dose of steroid therapy (prednisone or methylprednisolone) in improving symptoms of late radiation-associated lower cranial neuropathy in oropharyngeal cancer survivors. Steroid therapy with prednisone or methylprednisolone may help to improve symptoms associated with late radiation-associated lower cranial neuropathy.

NCT05136196 — BiCaZO: A Study Combining Two Immunotherapies (Cabozantinib and Nivolumab) to Treat Patients With Advanced Melanoma or Squamous Cell Head and Neck Cancer, an immunoMATCH Pilot Study

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment150
Study TypeINTERVENTIONAL
ConditionsClinical Stage III Cutaneous Melanoma AJCC v8; Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage IV Cutaneous Melanoma AJCC v8; Clinical Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Locally Recurrent Head and Neck Squamous Cell Carcinoma
Interventions; ;

This phase II trial studies the good and bad effects of the combination of drugs called cabozantinib and nivolumab in treating patients with melanoma or squamous cell head and neck cancer that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Cabozantinib may stop the growth of tumor cells by blocking some of the enzymes needed f…

NCT04695600 — Onabotulinum Toxin A (Botox) in the Treatment of Pharyngo-esophageal Dysphagia

StatusRecruiting
PhasePhase 2 / Phase 3
SponsorAll India Institute of Medical Sciences
Enrollment100
Study TypeINTERVENTIONAL
ConditionsTransfer Dysphagia; Oropharyngeal Dysphagia; Cricopharyngeus Muscle Dysfunction
Interventions

Dysphagia in patients with stroke, multiple sclerosis, parkinsonism or dystonia can occur due to relative hypertonia of the cricopharyngeus muscle. In the resting state, muscle is contracted and relaxes only during deglutition. Treatment of dysphagia by injecting botulinum toxin in the cricopharyngeus was described by Schneider et al. in 1994. More than 100 cases have been described after that,…

NCT06017895 — Doxepin Solution for Alleviation of Stubborn Breakthrough Pain Induced by Swallowing in Patients Receiving Radiotherapy for Nasopharyngeal Carcinoma

StatusRecruiting
PhaseN/A
SponsorNanfang Hospital, Southern Medical University
Enrollment178
Study TypeINTERVENTIONAL
ConditionsSwallowing-induced Pain
Interventions;

The goal of this clinical trial is to explore the effectiveness and adverse reactions of doxepin solution spray for alleviation of stubborn breakthrough pain induced by swallowing in patients receiving radiotherapy for nasopharyngeal carcinoma.

NCT06029270 — Testing the Addition of BMS-986016 (Relatlimab) to the Usual Immunotherapy After Initial Treatment for Recurrent or Metastatic Nasopharyngeal Cancer

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment156
Study TypeINTERVENTIONAL
ConditionsMetastatic Nasopharyngeal Carcinoma; Recurrent Nasopharyngeal Carcinoma; Stage IV Nasopharyngeal Carcinoma AJCC v8
Interventions; ;

This phase II trial tests the addition of BMS-986016 (relatlimab) to the usual immunotherapy after initial treatment for nasopharyngeal cancer that has come back after a period of improvement (recurrent) or that has spread from where it first started (primary site) to other places in the body (metastatic). Relatlimab is a monoclonal antibody that may interfere with the ability of tumor cells to…

NCT06592599 — Gemcitabine + Docetaxel + Toripalimab Induction in Epstein-Barr Virus (EBV) Associated Nasopharyngeal Carcinoma(NPC)

StatusRecruiting
PhasePhase 2
SponsorStanford University
Enrollment24
Study TypeINTERVENTIONAL
ConditionsNasopharyngeal Carcinoma
Interventions;

The purpose of the research is to test the safety and efficacy of the investigational drug in human subjects with cancer.

NCT06788002 — LDRT and Chemoimmunotherapy in NPC With Liver Metastasis

StatusRecruiting
PhasePhase 2
SponsorHunan Cancer Hospital
Enrollment26
Study TypeINTERVENTIONAL
ConditionsNasopharyngeal Cancinoma (NPC)
Interventions

This study aims to evaluate the efficacy and toxicity of adding low-dose radiotherapy to chemoimmunotherapy as a first-line treatment for nasopharyngeal carcinoma patients with liver metastasis.

NCT06543316 — Marginal Ulcer Healing With Low-Thermal Argon Plasma Endoscopic Treatment

StatusRecruiting
PhaseN/A
SponsorChristopher C. Thompson, MD, MSc
Enrollment100
Study TypeINTERVENTIONAL
ConditionsRoux-en-y Anastomosis Site; Marginal Ulcer; Marginal Ulcer (Peptic) or Erosion; Ulcer; Ulcer, Gastric
Interventions;

The objective of the study is to investigate the treatment of marginal ulcers with Low Thermal plasma in an endoscopic setting. By a treatment of the ulcerated areas with argon plasma with low power settings (~ 1 W) we hypothesize that the size of the ulcers will shrink, and the healing is accelerated compared to standard of care alone. Patients will benefit from this minimally invasive approa…

NCT06589804 — Testing the Addition of Anti-Cancer Drug, Cetuximab, to Standard of Care Treatment (Pembrolizumab) for Returning or Spreading Head and Neck Cancer After Previous Treatment

StatusRecruiting
PhasePhase 3
SponsorNational Cancer Institute (NCI)
Enrollment158
Study TypeINTERVENTIONAL
ConditionsMetastatic Head and Neck Squamous Cell Carcinoma; Metastatic Hypopharyngeal Squamous Cell Carcinoma; Metastatic Laryngeal Squamous Cell Carcinoma; Metastatic Oral Cavity Squamous Cell Carcinoma; Metastatic Oropharyngeal Squamous Cell Carcinoma
Interventions; ;

This phase III trial compares the effect of adding cetuximab to pembrolizumab versus pembrolizumab alone in treating patients with head and neck squamous cell carcinoma (HNSCC) that has come back after a period of improvement (recurrent) and/or that has spread from where it first started (primary site) to other places in the body (metastatic). Cetuximab is in a class of medications called monoc…

NCT06819228 — Window Trial of Fluorescently Labeled Panitumumab (Panitumumab-IRDye800) in Head and Neck Cancer

StatusRecruiting
PhasePhase 1
SponsorVanderbilt-Ingram Cancer Center
Enrollment60
Study TypeINTERVENTIONAL
ConditionsHNSCC; HNSCC,Larynx, Pharynx and Oral Cavity; SCC - Squamous Cell Carcinoma
Interventions

This study is exploring the use of Panitumumab in Head and Neck Cancer. Panitumumab is an approved drug named Vectibix and is used as an anti-cancer agent in other cancers such as colorectal cancer. It works by attaching to the cancer cell in a unique way that allows the drug to get into the cancer tissue. In addition to the Panitumumab, participants will also receive a Panitumumab-IRDye800 (Pa…

NCT06532279 — Testing the Addition of the Drug BMX-001, a Radioprotector, or a Placebo to the Usual Chemoradiation Therapy for Patients With Head and Neck Cancer

StatusRecruiting
PhasePhase 2
SponsorNRG Oncology
Enrollment98
Study TypeINTERVENTIONAL
ConditionsClinical Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Head and Neck Squamous Cell Carcinoma; Hypopharyngeal Squamous Cell Carcinoma
Interventions; ;

This phase II trial compares the effectiveness of adding BMX-001 to usual symptom management versus usual symptom management alone for reducing oral mucositis in patients who are receiving chemoradiation for head and neck cancer. Oral mucositis (inflammation and mouth sores) is a common side effect of chemoradiation that can cause pain and difficulty swallowing. Usual management of these side e…

NCT07124000 — DESTINY-PANTUMOUR04

StatusRecruiting
PhaseN/A
SponsorAstraZeneca
Enrollment100
Study TypeOBSERVATIONAL
ConditionsAdenocarcinoma (NOS); Anal Cancer; Bladder Cancer; Cervical Cancer; Endometrial Cancer
Interventions

This study will evaluate the effectiveness of T-DXd in patients with HER2-positive (IHC 3+) locally advanced, unresectable, or metastatic solid tumors who have received prior systemic treatment for metastatic or advanced disease and have no satisfactory alternative treatment options in a real-world setting in the US

NCT07195734 — Testing the Addition of Chemotherapy or Chemo-Immunotherapy to the Usual Surgery for Advanced Head and Neck Cancer

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment180
Study TypeINTERVENTIONAL
ConditionsClinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Locally Recurrent Head and Neck Squamous Cell Carcinoma; Locally Recurrent Hypopharyngeal Squamous Cell Carcinoma; Locally Recurrent Laryngeal Squamous Cell Carcinoma
Interventions; ;

This phase II trial tests the addition of chemotherapy, with carboplatin and paclitaxel, or chemo-immunotherapy, with carboplatin, paclitaxel and cemiplimab to standard salvage surgery followed by post operative radiation therapy and cisplatin for high risk patients, for the treatment of patients with PD-L1 positive head and neck squamous cell carcinoma that has come back and spread to nearby t…

NCT07451028 — Effect of an Oral Neuromuscular Training Device on Dysphagia

StatusRecruiting
PhaseN/A
SponsorUniversity of Aarhus
Enrollment100
Study TypeINTERVENTIONAL
ConditionsDysphagia
Interventions;

Dysphagia is a frequent complication following stroke, with an estimated prevalence of 42%. One training modality which have been implemented in both hospitals and municipalities for alleviating dysphagia are oral neuromuscular training devices. These devices are hand-held acrylic devices which are inserted between the lips and teeth by the patient or an assistant and pulled forward against lip…

NCT07678086 — Effect of Endotracheal Tube Cuff Pressure Management on Postoperative Sore Throat in Pediatric Laparoscopic Appendectomy

StatusRecruiting
PhaseN/A
SponsorAnkara Etlik City Hospital
Enrollment60
Study TypeINTERVENTIONAL
ConditionsAppendicitis Acute; Postoperative Sore Throat, Cough, Hoarseness; Airway Complications; Respiratory Complications
Interventions;

Abstract Objective:

The aim of this study is to compare two different ways of adjusting the air-filled cushion (cuff) of the breathing tube used during general anesthesia in children undergoing laparoscopic appendectomy (closed surgery for appendicitis). The goal is to see if maintaining the pressure in this cushion within a safe, specific range (15-18 mmHg) helps prevent or reduce sore throat…

NCT07027826 — The Esophageal String Test as a Diagnostic Screening Tool for Eosinophilic Esophagitis Among Africans With Dysphagia in Mali and the United States

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment70
Study TypeINTERVENTIONAL
ConditionsDysphagia; Eosinophilic Esophagitis
Interventions

Background:

Eosinophilic esophagitis (EoE) is a disease that causes inflammation in the esophagus. The esophagus is the tube that moves food from the mouth to the stomach. Diagnosing EoE currently requires a specialized tool called an endoscope. The esophageal string test (EST) is another test; the EST collects fluid from the upper digestive tract. An EST is simpler and cheaper than an endosco…

Active, Not Recruiting

NCT02135042 — Individualized Treatment Treating Patients With Stage II-IVB Nasopharyngeal Cancer Based on EBV DNA

StatusActive, not recruiting
PhasePhase 2 / Phase 3
SponsorNRG Oncology
Enrollment685
Study TypeINTERVENTIONAL
ConditionsEpstein-Barr Virus Infection; Stage II Nasopharyngeal Carcinoma; Stage III Nasopharyngeal Carcinoma; Stage IVA Nasopharyngeal Carcinoma; Stage IVB Nasopharyngeal Carcinoma
Interventions; ;

There are two study questions we are asking in this randomized phase II/III trial based on a blood biomarker, Epstein Barr virus (EBV) deoxyribonucleic acid (DNA) for locoregionally advanced non-metastatic nasopharyngeal cancer. All patients will first undergo standard concurrent chemotherapy and radiation therapy. When this standard treatment is completed, if there is no detectable EBV DNA in …

NCT03097939 — Phase 2 Trial of Ipilimumab and Nivolumab in Nasopharyngeal Carcinoma

StatusActive, not recruiting
PhasePhase 2
SponsorNational Cancer Centre, Singapore
Enrollment113
Study TypeINTERVENTIONAL
ConditionsNasopharyngeal Carcinoma
Interventions;

The purpose of this study is to test the hypothesis that a combined Immuno-Oncology (IO) strategy would see efficacy in a virally driven cancer like Nasopharyngeal Carcinoma (NPC). Hence, this is a combination study of nivolumab and ipilimumab in Epstein-Barr virus (EBV) driven nasopharyngeal carcinoma.

NCT03729518 — TORS De-Intensification Protocol Version 2.0: Dose and Volume Reduction in the Neck

StatusActive, not recruiting
PhaseN/A
SponsorAbramson Cancer Center at Penn Medicine
Enrollment150
Study TypeINTERVENTIONAL
ConditionsOropharyngeal Cancer; Squamous Cell Carcinoma; Human Papilloma Virus
Interventions

This is a single-arm Phase II study of adjuvant radiation for locally advanced p16+ oropharyngeal squamous cell carcinoma. The main purpose of this research is to determine the likelihood of cancer growing back in the throat or in the neck two years after completion of radiation if lower doses of radiation are used to a smaller area of the head and neck region than is currently used in standard…

NCT03811015 — Testing Immunotherapy Versus Observation in Patients With HPV Throat Cancer

StatusActive, not recruiting
PhasePhase 3
SponsorNational Cancer Institute (NCI)
Enrollment636
Study TypeINTERVENTIONAL
ConditionsClinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8
Interventions; ;

This phase III trials studies whether maintenance immunotherapy (nivolumab) following definitive treatment with radiation and chemotherapy (cisplatin) result in significant improvement in overall survival (time being alive) and progression-free survival (time being alive without cancer) for patients with intermediate risk human papillomavirus (HPV) positive oropharynx cancer (throat cancer) tha…

NCT03952585 — De-intensified Radiation Therapy With Chemotherapy (Cisplatin) or Immunotherapy (Nivolumab) in Treating Patients With Early-Stage, HPV-Positive, Non-Smoking Associated Oropharyngeal Cancer

StatusActive, not recruiting
PhasePhase 2 / Phase 3
SponsorNational Cancer Institute (NCI)
Enrollment384
Study TypeINTERVENTIONAL
ConditionsBasaloid Squamous Cell Carcinoma; Clinical Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Oropharyngeal Squamous Cell Carcinoma; Papillary Squamous Cell Carcinoma
Interventions; ;

This phase II/III trial studies how well a reduced dose of radiation therapy works with nivolumab compared to cisplatin in treating patients with human papillomavirus (HPV)-positive oropharyngeal cancer that is early in its growth and may not have spread to other parts of the body (early-stage), and is not associated with smoking. Radiation therapy uses high-energy x-rays to kill tumor cells an…

NCT04862650 — Cemiplimab, Low-Dose Paclitaxel and Carboplatin for the Treatment of Recurrent/Metastatic Squamous Cell Carcinoma of the Head and Neck

StatusActive, not recruiting
PhasePhase 2
SponsorMarcelo Bonomi
Enrollment46
Study TypeINTERVENTIONAL
ConditionsClinical Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Metastatic Head and Neck Squamous Cell Carcinoma; Metastatic Hypopharyngeal Squamous Cell Carcinoma; Metastatic Laryngeal Squamous Cell Carcinoma; Metastatic Oral Cavity Squamous Cell Carcinoma
Interventions; ;

This phase II trial studies the effect of cemiplimab in combination with low-dose paclitaxel and carboplatin in treating patients with squamous cell carcinoma of the head and neck that has come back (recurrent) or spread to other places in the body (metastatic). Immunotherapy with monoclonal antibodies, such as cemiplimab , may help the body’s immune system attack the cancer, and may interfere …

NCT04925544 — Novel Small Molecule EBNA1 Inhibitor, VK 2019, in Patients With Epstein Barr Virus (EBV)-Positive Nasopharyngeal Cancer (NPC) and Other Epstein-Barr Virus (EBV)-Associated Cancers, With Pharmacokinetic and Pharmacodynamic Correlative Studies

StatusActive, not recruiting
PhasePhase 2
SponsorStanford University
Enrollment13
Study TypeINTERVENTIONAL
ConditionsNasopharyngeal Cancer; Epstein-Barr Virus Related Carcinoma
Interventions

To evaluate the anti cancer effect of VK 2019 in subjects with EBV related nasopharyngeal carcinoma (NPC) for whom there is no other standard treatment available

NCT05063552 — Testing the Use of Investigational Drugs Atezolizumab and/or Bevacizumab With or Without Standard Chemotherapy in the Second-Line Treatment of Advanced-Stage Head and Neck Cancers

StatusActive, not recruiting
PhasePhase 2 / Phase 3
SponsorNational Cancer Institute (NCI)
Enrollment430
Study TypeINTERVENTIONAL
ConditionsClinical Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Metastatic Head and Neck Squamous Cell Carcinoma; Metastatic Hypopharyngeal Squamous Cell Carcinoma; Metastatic Laryngeal Squamous Cell Carcinoma; Metastatic Lip and Oral Cavity Carcinoma
Interventions; ;

This phase II/III compares the standard therapy (chemotherapy plus cetuximab) versus adding bevacizumab to standard chemotherapy, versus combination of just bevacizumab and atezolizumab in treating patients with head and neck cancer that has spread to other places in the body (metastatic or advanced stage) or has come back after prior treatment (recurrent). Immunotherapy with monoclonal antibod…

NCT05813626 — Neoadjuvant Chemotherapy Plus Toripalimab in Patients With Locoregionally Advanced Nasopharyngeal Carcinoma

StatusActive, not recruiting
PhasePhase 2
SponsorZhejiang Cancer Hospital
Enrollment89
Study TypeINTERVENTIONAL
ConditionsNasopharyngeal Carcinoma
Interventions; ;

Neoadjuvant chemotherapy plus toripalimab in patients with locoregionally advanced nasopharyngeal carcinoma

NCT05721755 — Combining Radiation Therapy With Immunotherapy for the Treatment of Metastatic Squamous Cell Carcinoma of the Head and Neck

StatusActive, not recruiting
PhasePhase 3
SponsorECOG-ACRIN Cancer Research Group
Enrollment290
Study TypeINTERVENTIONAL
ConditionsClinical Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Metastatic Head and Neck Squamous Cell Carcinoma; Metastatic Hypopharyngeal Squamous Cell Carcinoma; Metastatic Laryngeal Squamous Cell Carcinoma; Metastatic Oral Cavity Squamous Cell Carcinoma
Interventions; ;

This phase III trial compares pembrolizumab with radiation therapy to pembrolizumab without radiation therapy (standard therapy) given after pembrolizumab plus chemotherapy for the treatment of patients with squamous cell carcinoma of the head and neck that has spread from where it first started (primary site) to other places in the body (metastatic). Pembrolizumab is a type of immunotherapy th…

NCT07670429 — Longitudinal Ultrasound Kinematic Evaluation of Digastric Muscles

StatusActive, not recruiting
PhaseN/A
SponsorHopital Forcilles
Enrollment70
Study TypeOBSERVATIONAL
ConditionsSwallowing

Ultrasound applied to the upper aerodigestive tract for the assessment of swallowing disorders has been the subject of numerous publications in recent years. Changes in the range of motion or muscular characteristics of the structures involved in swallowing are associated with the presence of swallowing disorders. However, current assessment remains limited to morphological parameters at rest, …

Not Yet Recruiting

NCT07674706 — Evaluating the Optimal Timing of Acupuncture for Managing Chemoradiation-induced Xerostomia in Patients With Head and Neck Cancers

StatusNot yet recruiting
PhaseN/A
SponsorNational University Hospital, Singapore
Enrollment50
Study TypeINTERVENTIONAL
ConditionsXerostomia; Head Cancer; Neck Cancer; Nasopharyngeal Carcinoma (NPC); Oral Cavity Squamous Cell Carcinoma
Interventions

While existing data supports the use of acupuncture to reduce radiation-induced xerostomia, the optimal timing of acupuncture for managing chemoradiation-induced xerostomia remains an area of active investigation. Prior studies have administered acupuncture either in patients who developed xerostomia 12 months after radiation 10 or during the radiation therapy itself 9. The hypothesis is that a…

NCT07656025 — Efficacy and Mechanism of ‘Yanjiu Needle’ for Pharyngeal Dysphagia Based on sEMG Features

StatusNot yet recruiting
PhaseN/A
SponsorThe Third People’s Hospital of Huizhou
Enrollment100
Study TypeINTERVENTIONAL
ConditionsAcupuncture; Dysphagia; Surface EMG
Interventions; ;

Dysphagia is one of the most common and serious complications following stroke. It can easily lead to aspiration and aspiration pneumonia, reduce patients’ quality of life, increase healthcare costs, and result in high mortality rates, making it a clinical issue that urgently needs to be addressed. Current mainstream therapies have limitations: neurostimulation targets a single pathway, while r…

NCT07475091 — Standardizing Swallow Pressure Measurements

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Wisconsin, Madison
Enrollment25
Study TypeINTERVENTIONAL
ConditionsDysphagia
Interventions;

This study aims to directly compare and contrast swallowing pressure and impedance measurements obtained from two high-resolution manometry (HRM) systems: the Laborie LMT Pharyngeal System and the Medtronic ManoScan ESO HRM System in healthy adult volunteers. The primary objective is to determine how differences in catheter diameter, sensor configuration, and acquisition platforms influence mea…

NCT07578727 — A Multicenter, Prospective, Phase III Clinical Study of Proton Intensity-modulated Radiotherapy Versus Photon Intensity-modulated Radiotherapy for Untreated Non-metastatic Nasopharyngeal Carcinoma

StatusNot yet recruiting
PhaseN/A
SponsorGuangzhou Concord Cancer Center
Enrollment504
Study TypeINTERVENTIONAL
ConditionsNasopharyngeal Carcinoma (NPC)
Interventions;

Proton therapy for nasopharyngeal carcinoma can reduce radiotherapy-related toxic reactions, and some retrospective studies have found that proton therapy improves the survival of patients with nasopharyngeal carcinoma. However, high-level prospective clinical evidence is still lacking. This study aims to investigate the efficacy and side effects of proton therapy compared with photon intensity…

NCT07684105 — Treatment of Dysphagia in Patients With Dystrophic Epidermolysis Bullosa With Budesonide: a Retrospective Bicentric Study Nice - Paris St Louis / Necker (EBUDE Study)

StatusNot yet recruiting
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nice
Enrollment15
Study TypeINTERVENTIONAL
ConditionsRecessive Dystrophic Epidermolysis Bullosa; Dysphagia; Esophageal Stenosis
Interventions

Budesonide is an anti-inflammatory medication that works by decreasing the immune system’s overreaction. In the treatment of eosinophilic esophagitis, especially with Jorveza or a preparation made in a pharmacy, it reduces the production of substances responsible for inflammation in the esophagus. This action reduces the accumulation of certain inflammatory cells (eosinophils) and thus improves…

NCT07667400 — Docetaxel and SX-682 in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma, Salivary Gland Carcinoma, and Advanced Prostate Cancer

StatusNot yet recruiting
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment120
Study TypeINTERVENTIONAL
ConditionsHead and Neck Cancer; Head and Neck Squamous Cell Carcinoma; Paranasal Sinus Neoplasms; Nasopharyngeal Carcinoma; Oropharyngeal Squamous Cell Carcinoma
Interventions;

Background:

Head and neck cancers (HNCs) account for about 5% of all cancers worldwide. They grow in the mouth, throat, nasal cavity, or salivary glands. Prostate cancer is the most common cancer in men in the United States. Survival rates for these cancers are lower than 50% if they spread to other parts of the body or return after treatment. Better treatments are needed.

Objective:

To test…

NCT07671014 — Metagenomic Analysis of the Pharynx in High Risk Partners

StatusNot yet recruiting
PhaseN/A
SponsorGuy’s and St Thomas’ NHS Foundation Trust
Enrollment100
Study TypeOBSERVATIONAL
ConditionsGonorrhea; Neisseria Gonorrhea; Neisseria Meningitidis; Metagenomic Next Generation Sequencing

The Neisseria gonorrhoea (NG) epidemic in England is at the highest level in one hundred years of public health records. The World Health Organisation has listed NG as one of the top five bacterial infections globally because of the ability of the bacteria to develop resistance to antibiotics. Neisseria meningitidis (NM) is a common pharyngeal commensal and it has been shown to be in one in fiv…

NCT07690618 — Thermotherapy for Head and Neck Cancer Patients

StatusNot yet recruiting
PhasePhase 1
SponsorErasmus Medical Center
Enrollment30
Study TypeINTERVENTIONAL
ConditionsHead and Neck Cancer; Oropharyngeal Carcinoma; Hypopharyngeal Carcinoma; Laryngeal Carcinoma; Head and Neck Squamous Cell Carcinoma
Interventions; ;

This phase I, single-center study evaluates the safety, tolerability, and recommended phase II dose (RP2D) of mild hyperthermia (thermotherapy) when added to standard-of-care treatment in patients with locally advanced head and neck squamous cell carcinoma (LAHNSCC). Tumor recurrence remains common despite chemoradiotherapy, highlighting the need for treatment intensification. Thermotherapy, wh…

NCT07429890 — REVIVE Prospective Registry Cohort Study

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of California, Davis
Enrollment31
Study TypeOBSERVATIONAL
ConditionsOropharyngeal Dysphagia
Interventions

The main purpose of this registry is to collect observational, long-term safety and effectiveness data in participants who have received iltamiocel as part of the blinded portion of the REVIVE clinical study.

NCT07631364 — Efficacy of Temocillin Compared to Standard of Care in the Treatment of Neisseria Gonorrhoeae Infections

StatusNot yet recruiting
PhasePhase 3
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment360
Study TypeINTERVENTIONAL
ConditionsNeisseria Gonorrhoeae (Ng) Infections
Interventions; ;

Neisseria gonorrhoeae (Ng) infections are common and increasing in incidence. Treatment with a third generation cephalosporin, i.e ceftriaxone 1g, single dose, intramuscular (IM), is recommended as a first line treatment. Ceftriaxone is a broad-spectrum antibiotic with high impact on the intestinal microbiota associated with the acquisition of multidrug-resistant bacteria, particularly extended…

Enrolling by Invitation

NCT04266093 — Gene Therapy Follow up Protocol for Subjects Previously Enrolled in NCI Center for Immuno-Oncology Studies

StatusEnrolling by invitation
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsCervical Intraepithelial Neoplasia; Cervical Neoplasms; Oropharyngeal Neoplasms; Squamous Intraepithelial Lesions of the Cervix; Hematologic Malignacies
Interventions

Background:

Gene therapy is closely followed by the U.S. Food and Drug Administration (FDA). The FDA requires researchers to conduct long-term follow-up of people who have had the treatment. This study collects data on people who have had gene therapy and sends it to the FDA. The data does not include participants names.

Objective:

To contact current or past participants of gene therapy prot…

Completed Trials

NCT01150721 — Comparing Expectorated and Induced Sputum and Pharyngeal Swabs for Cultures, AFB Smears, and Cytokines in Pulmonary Nontuberculous Mycobacterial Infection

StatusCompleted
PhaseN/A
SponsorNational Institutes of Health Clinical Center (CC)
Enrollment177
Study TypeOBSERVATIONAL
ConditionsMycobacterium Infections, Non-tuberculous

Background:

- Pulmonary nontuberculous mycobacterial infection is a respiratory infection that is sometimes difficult to diagnose. Proper diagnosis depends on accurate collection of respiratory secretions, but these secretions may be contaminated by bacteria present in the mouth at the time of collection. In addition, some individuals may have difficulty providing respiratory secretions, beca…

NCT04528394 — Proton Versus Photon Radiotherapy for Nasopharyngeal Carcinoma

StatusCompleted
PhasePhase 2
SponsorShanghai Proton and Heavy Ion Center
Enrollment136
Study TypeINTERVENTIONAL
ConditionsNasopharyngeal Carcinoma
Interventions; ;

The purpose of this study is to compare the toxicity and therapeutic efficacy of proton or photon combined with carbon ion radiotherapy for newly diagnosed nasopharyngeal carcinoma.Participants will be randomized to 2 arms. Arm 1, participants received photon combined with carbon ion radiotherapy group, Arm 2, participants received proton combined with carbon ion radiotherapy.

NCT04287868 — Combination Immunotherapy in Subjects With Advanced HPV Associated Malignancies

StatusCompleted
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment51
Study TypeINTERVENTIONAL
ConditionsCervical Cancer; HPV Cancers; Anal Cancer; Oropharyngeal Cancer; Vulvar, Vaginal, Penile, Rectal Cancer
Interventions; ;

Background:

More than 30,000 cases of human papillomavirus (HPV) associated cancers occur annually in the United States. When these cancers spread, they do not respond well to standard treatments and are often incurable. Researchers want to see if a mix of drugs can help.

Objective:

To learn if a mix of immunotherapy drugs can shrink tumors in people with HPV associated cancers.

Eligibility…

NCT04889898 — Remote Speech and Swallowing Assessment in ALS

StatusCompleted
PhaseN/A
SponsorMilton S. Hershey Medical Center
Enrollment200
Study TypeOBSERVATIONAL
ConditionsAmyotrophic Lateral Sclerosis
Interventions; ;

The investigators propose a longitudinal home study of ALS patients to measure the severity of speech and swallowing (bulbar) impairment via a smartphone-based, remote speech and swallow assessment (rSSA). The study is designed to assess the feasibility and validity of such a monitoring intervention. Furthermore, it is proposed that regular monitoring of these two bulbar processes may shed ligh…

NCT05882890 — Does Craniosacraltherapy Combined With Exercises That Focuses om Respiration and Posture in the Upper Body Have an Effect on Xerostomia and Other Late Sequelae on People Who Has Been Suffering From Cancer in Mouth and Throat?

StatusCompleted
PhaseN/A
SponsorCathrine Rahbek
Enrollment11
Study TypeINTERVENTIONAL
ConditionsXerostomia Following Radiotherapy; Xerostomia Following in Neck or Head After Cancer Surgery; Other Late Sequelae Following Radiotherapy and Cancer Surgery in Neck or Head
Interventions;

The current study aims to assess the efficacy of manual treatment with craniosacral therapy of fascial tissue in throat, neck, cranial and mouth region, on radiation and/or surgery-induced salivary gland hypofunction and xerostomia in patients who have received surgery and/or radiation therapy because of cancer in the throat and mouth regions.

The hypothesis of this project is based on a recen…

NCT05998902 — Optimizing Early Nutrition Support in Severe Stroke-2

StatusCompleted
PhasePhase 3
SponsorWen Jiang-3
Enrollment546
Study TypeINTERVENTIONAL
ConditionsSevere Stroke; Acute Stroke; Dysphagia
Interventions;

Post stroke pneumonia (PSP) is one of the common early complications of stroke. Post-stroke infections, in general, are associated with less favorable neurologic outcomes. Aspiration is one of the most feared complications of enteral nutrition and can lead to the occurrence of pneumonia. Severe stroke patients are at high risk for aspiration due to some factors such as the reduced level of cons…

NCT07675278 — Comparing Two Agents Used to Stop Bleeding During Tonsil Removal Surgery: Adrenaline Versus Hydrogen Peroxide

StatusCompleted
PhaseN/A
SponsorRawalpindi Medical College
Enrollment64
Study TypeINTERVENTIONAL
ConditionsChronic Tonsillitis; Tonsillar Hypertrophy, Tonsillitis; Tonsillectomy
Interventions;

The goal of this quasi-experimental study is to compare the effectiveness of topical adrenaline and 3% hydrogen peroxide for controlling bleeding (hemostasis) during tonsil removal surgery in patients aged 5 to 18 years. The main questions it aims to answer are: 1. Which substance leads to faster bleeding control during surgery? 2. Which substance results in less total blood loss during surgery…

NCT06615310 — Ultrasonographic Parameters in Stroke Patients With Dysphagia

StatusCompleted
PhaseN/A
SponsorIstanbul Physical Medicine Rehabilitation Training and Research Hospital
Enrollment52
Study TypeOBSERVATIONAL
ConditionsStroke; Dysphagia
Interventions

ultrasonographic parameters in stroke patients with dysphagia

NCT07656844 — Motor Imagery in Post-Stroke Dysphagia

StatusCompleted
PhaseN/A
SponsorAnkara Etlik City Hospital
Enrollment43
Study TypeINTERVENTIONAL
ConditionsPost-stroke Dysphagia; Oropharyngeal Dysphagia (OPD)
Interventions; ;

This study evaluated the effects of motor imagery added to conventional swallowing rehabilitation in patients with dysphagia after stroke. Dysphagia, or swallowing difficulty, is a common problem after stroke and may increase the risk of aspiration, pneumonia, malnutrition, dehydration, and reduced quality of life.

Participants with post-stroke dysphagia were randomly assigned to one of three …

Other (Suspended)

NCT05050162 — Comparing Cisplatin Every Three Weeks to Cisplatin Weekly When Combined With Radiation for Patients With Advanced Head and Neck Cancer

StatusSuspended
PhasePhase 2 / Phase 3
SponsorNRG Oncology
Enrollment1714
Study TypeINTERVENTIONAL
ConditionsAdvanced Head and Neck Squamous Cell Carcinoma; Advanced Hypopharyngeal Squamous Cell Carcinoma; Advanced Laryngeal Squamous Cell Carcinoma; Advanced Oropharyngeal Squamous Cell Carcinoma; Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8
Interventions; ;

This phase II/III trial compares whether cisplatin given weekly with radiation therapy is better tolerated than cisplatin given every three weeks with radiation therapy for the treatment of head and neck cancer that has spread to other places in the body (advanced). The second part of this study will also help to find out if the cisplatin given weekly approach will extend patients’ life by at l…