Clinical Trials for Swallowing Disorders

Currently registered clinical trials for Swallowing Disorders from ClinicalTrials.gov. 20 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 Swallowing Disorders from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 20
  • Active, not recruiting: 5
  • Completed: 11
  • Other: 14

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

Recruiting Trials

NCT04506593 — Indiana University Gastrointestinal Motility Diagnosis Registry

StatusRecruiting
PhaseN/A
SponsorIndiana University
Enrollment5000
Study TypeOBSERVATIONAL
ConditionsEosinophilic Esophagitis; Gastroesophageal Reflux Disease (GERD); Gastroparesis; Functional Vomiting; Irritable Bowel Syndrome (IBS)
Interventions

Develop a registry (list of patients) with accurate clinical motility diagnosis. This registry will help the doctors to identify the patients with specific disease conditions. It will also help in promoting future research in gastroenterology motility disorders

NCT04503785 — Esophageal Impedance and Manometry Measurements and Dysphagia Symptom Scoring

StatusRecruiting
PhaseN/A
SponsorIndiana University
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsDysphagia, Esophageal
Interventions

Comparison of manometry measurements and EndoFlip Balloon measurements in patients with dysphagia and a known esophageal diagnosis

NCT05469854 — A Study to Investigate the Pharmacokinetics and ECG Effects of Linaprazan Glurate

StatusRecruiting
PhasePhase 1
SponsorCinclus Pharma Holding AB
Enrollment121
Study TypeINTERVENTIONAL
ConditionsPharmacokinetics; Cardiodynamic ECG; Safety, and Tolerability; GERD
Interventions;

This is a Phase I, single-center, double blind, placebo-controlled, parallel-group, randomized trial designed to evaluate the PK, cardiodynamic ECG effects, safety, and tolerability of single oral doses of linaprazan glurate. The trial will explore the PK properties of linaprazan glurate and linaprazan as well as the cardiodynamic ECG effects, safety, and tolerability after the administration o…

NCT05496998 — Transcatheter Mitral Valve Replacement in Patients With Severe Symptomatic Mitral Regurgitation - APOLLO-EU Trial

StatusRecruiting
PhaseN/A
SponsorMedtronic Cardiovascular
Enrollment400
Study TypeINTERVENTIONAL
ConditionsMitral Regurgitation
Interventions

Evaluate the safety and efficacy of Medtronic Intrepid™ TMVR TF System in patients with moderate-to-severe or severe symptomatic mitral regurgitation, or moderate symptomatic mitral regurgitation combined with mitral stenosis in the presence of MAC who, by agreement of the local site multidisciplinary heart team experienced in mitral valve therapies, are unsuitable for treatment with approved t…

NCT07678177 — An Observational Study to Evaluate the Efficacy and Safety of K-CAB Tab./K-CAB ODT(Tegoprazan) in GERD Patients

StatusRecruiting
PhaseN/A
SponsorHK inno.N Corporation
Enrollment5384
Study TypeOBSERVATIONAL
ConditionsGERD (Gastroesophageal Reflux Disease)

This study aims to evaluate the status of AE and improvement effect of K-CAB Tab/K-CAB ODT(Tegoprazan) 50mg in patients with GERD.

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.

NCT05777512 — Randomized Controlled Crossover Trial of Postpyloric Feedings to Improve Pulmonary Outcomes in High-risk Preterm Infants

StatusRecruiting
PhaseN/A
SponsorBoston Children’s Hospital
Enrollment50
Study TypeINTERVENTIONAL
ConditionsBronchopulmonary Dysplasia
Interventions;

The purpose of this study is to determine if postpyloric feedings effectively improve objective measures of pulmonary health in preterm infants with chronic lung disease when compared with nasogastric (NG) feedings. This research will (1) determine the optimal nutritional management to prevent a common and costly complication of prematurity, and (2) use a novel crossover design that examines ou…

NCT06613438 — Safety and Effectiveness of eGERD Device to Reduce Gastroesophageal Reflux Disease (GERD) Symptoms

StatusRecruiting
PhaseN/A
SponsorGerd Care Medical Ltd
Enrollment84
Study TypeINTERVENTIONAL
ConditionsGERD (Gastroesophageal Reflux Disease)
Interventions;

The purpose of this research is to evaluate the safety and effectiveness of the eGERD device, which is a novel device for treating Gastroesophageal Reflux Disease (GERD).

The main questions this research aims to answer are:

  1. Does the eGERD device reduce acidity in the esophagus?
  2. Does the eGERD device reduce GERD symptoms such as heartburn and regurgitation?
  3. What medical problems do pa…

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…

NCT06534359 — Transpyloric Versus Gastric Feeding in Bronchopulmonary Dysplasia

StatusRecruiting
PhaseN/A
SponsorChildren’s Hospital of Philadelphia
Enrollment60
Study TypeINTERVENTIONAL
ConditionsBronchopulmonary Dysplasia; Gastroesophageal Reflux
Interventions;

The goal of this clinical trial is to learn if transpyloric tube feeding (feeding directly into the small intestine) versus gastric tube feeding tolerably and effectively reduces gastroesophageal reflux in infants born premature who have been diagnosed with bronchopulmonary dysplasia. The main questions this trial aims to answer are:

Does transpyloric as compared to gastric tube feeding result…

NCT07069673 — Abbott Cephea Mitral Valve Disease Registry

StatusRecruiting
PhaseN/A
SponsorAbbott Medical Devices
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsMitral Regurgitation; Mitral Stenosis; Mitral Valve Disease; Mitral Valve (MV) Regurgitation; Mitral Annulus Calcification

The objective of this registry is to gather clinical data on symptomatic patients with mitral valve disease, including patients with mitral regurgitation, mitral stenosis, and mixed mitral valve disease. Data collected from this registry are expected to improve our understanding of the impact of correcting symptomatic mitral valve disease on clinical outcomes in patients that could be candidate…

NCT07125521 — Evaluating Medication Adherence of Patients With Gastroesophageal Reflux Disease With Support of the Smartphone Application GERDCare

StatusRecruiting
PhaseN/A
SponsorInstitute of Gastroenterology and Hepatology, Vietnam
Enrollment380
Study TypeINTERVENTIONAL
ConditionsGERD (Gastroesophageal Reflux Disease)
Interventions

Adherence to GERD treatment, including medication, diet, and lifestyle, is essential for symptom control and complication prevention, yet adherence rates remain low due to various demographic and clinical factors. Digital therapeutics, particularly mobile health applications, have shown promising potential in supporting chronic disease management and improving patient outcomes.

The GERDCare mo…

NCT07614633 — Natural History of Eosinophilic Esophagitis in Adult and Pediatric Population

StatusRecruiting
PhaseN/A
SponsorFondazione IRCCS Policlinico San Matteo di Pavia
Enrollment200
Study TypeOBSERVATIONAL
ConditionsEosinophilic Esophagitis (EoE)

Eosinophilic esophagitis (EoE) is a Th2-mediated disease induced by ingestion of ambiental and alimentary allergens. Incidence of EoE is increasing in recent years. Young male subjects are more often affected by EoE. Esophageal eosinophilic infiltrate causes different symptoms of esophageal dysfunction (i.e. dysphagia, food impaction, chest pain, heartburn). In pediatric population symptoms are…

NCT07291700 — Study on Hydrotalcite for Relief of Acid Symptoms Due to Acid Rebound After Stopping Long-Term PPI Therapy

StatusRecruiting
PhaseN/A
SponsorBayer
Enrollment167
Study TypeOBSERVATIONAL
ConditionsGastroesophageal Reflux
Interventions

This observational study aims to explore the effectiveness of hydrotalcite, marketed as Talcid, in alleviating acid-related symptoms that occur due to an acid rebound after discontinuing a non-/no-longer-indicated long-term proton pump inhibitor (PPI) therapy. PPIs are commonly prescribed to reduce stomach acid to alleviate symptoms such as heartburn and for the treatment of, for example, duode…

NCT07110142 — Tongue Proactive Strengthening Exercise Program Following Partial/Hemi Glossectomy and Reconstruction

StatusRecruiting
PhaseN/A
SponsorCase Comprehensive Cancer Center
Enrollment40
Study TypeINTERVENTIONAL
ConditionsOral Cancer; Head and Neck Cancer
Interventions

This study is being done to determine whether adding a proactive tongue strengthening exercise program using a biofeedback device (the Tongueometer) improves speech and swallowing outcomes after surgery for tongue cancer. Patients who undergo partial or hemiglossectomy often experience difficulties with speech and swallowing, which can significantly impact their quality of life. While speech an…

NCT07496840 — Clinical Outcomes, Safety, and Effectiveness of Speedboat UltraSlim™ in Per-Oral Endoscopic Myotomy (POEM)

StatusRecruiting
PhaseN/A
SponsorBaylor College of Medicine
Enrollment40
Study TypeOBSERVATIONAL
ConditionsEsophageal Motility Disorders; Achalasia

This study is a prospective registry designed to evaluate the clinical outcomes, safety, and effectiveness of per-oral endoscopic myotomy (POEM) performed using the Speedboat UltraSlim™ device in patients with achalasia or other esophageal motility disorders.

Participants included in this registry are those undergoing clinically indicated POEM as part of standard of care. No experimental inter…

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…

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…

NCT04383262 — Fosamprenavir for Laryngopharyngeal Upper Airway Tissue Treatment and Enzyme Reduction

StatusRecruiting
PhasePhase 2
SponsorMedical College of Wisconsin
Enrollment104
Study TypeINTERVENTIONAL
ConditionsLaryngopharyngeal Reflux
Interventions;

Laryngopharyngeal Reflux (LPR) is a common condition that causes symptoms like chronic cough, throat clearing, hoarseness, and trouble swallowing. If not treated, LPR can lead to long-term throat damage and may increase the risk of throat cancer. More than 20% of the people in the United States are estimated to have LPR, yet there is no effective medication approved to treat it. Drugs called pr…

Active, Not Recruiting

NCT00431756 — Novel Biomarkers in the Neoplastic Progression of Barrett’s Esophagus

StatusActive, not recruiting
PhaseN/A
SponsorJohns Hopkins University
Enrollment600
Study TypeOBSERVATIONAL
ConditionsBarrett Esophagus; Esophageal Neoplasm; Gastroesophageal Reflux

The purpose of this study is to determine if there are any early changes in DNA markers of blood and esophageal tissue in people with gastric reflux, Barrett’s esophagus or esophageal cancer that can warn of a progression to esophageal cancer.

NCT03705416 — Long Term Outcomes of Bariatric Patients Treated With Surgery or Endoscopy

StatusActive, not recruiting
PhaseN/A
SponsorJohns Hopkins University
Enrollment250
Study TypeOBSERVATIONAL
ConditionsGERD; Obesity
Interventions;

GERD is common in the obese population. Bariatric procedures are the mainstay of therapy for these patients. Bariatric procedures can be surgical (Roux-en-Y gastric bypass and Vertical sleeve gastrectomy) or endoscopic (endoscopic sleeve gastroplasty). The rate of GERD after either treatment is unknown as is the rate of silent reflux. The study primary objective is to assess the incidence rate …

NCT04253392 — RETHINK REFLUX Registry

StatusActive, not recruiting
PhaseN/A
SponsorEthicon Endo-Surgery
Enrollment500
Study TypeOBSERVATIONAL
ConditionsGastroesophageal Reflux
Interventions

The RETHINK REFLUX Registry is a post-market prospective, multi-center, observation, single arm, long-term safety surveillance registry of subjects implanted with the LINX device. The primary objective of the study is to confirm the long-term safety profile of the LINX device and procedure (implant/explant) up to 10 years post-implant.

NCT04450628 — Esophagogastric Junction Distensibility During Hiatal Hernia Repair

StatusActive, not recruiting
PhaseN/A
SponsorWake Forest University Health Sciences
Enrollment25
Study TypeINTERVENTIONAL
ConditionsEsophagogastric Junction Distensibility; Hiatal Hernia
Interventions

The investigators aim to ascertain the effects of hiatal hernia repair and fundoplication on the distensibility of the esophagogastric junction (EGJ) as measured by FLIP topography/impedance planimetry. The investigators also aim to assess for any correlation between values of EGJ distensibility and GERD related quality of life (QOL) and dysphagia scores.

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

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…

NCT07686471 — Short Versus Long Submucosal Tunneling in Per-oral Endoscopic Myotomy (POEM) for Type II Achalasia.

StatusNot yet recruiting
PhaseN/A
SponsorAssiut University
Enrollment50
Study TypeINTERVENTIONAL
ConditionsEsophageal Achalasia
Interventions

this study is prospective , randomized and interventional ,will be performed on 50 patients to compare the clinical utility , safety profile and postoperative recovery metrics between short and long per-oral endoscopic myotomy , patients will be divided randomly into two equal groups one will do short myotomy and the other group will do long myotomy , each group will contain 25 patients methodo…

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…

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…

NCT07667894 — Mindfulness Intervention for Emotional Distress (MIED) in Patients With GERD

StatusNot yet recruiting
PhaseN/A
SponsorXinghua Liu
Enrollment500
Study TypeINTERVENTIONAL
ConditionsGastroesophageal Reflux Disease; Emotional Distress
Interventions;

The goal of this multicenter randomized waitlist-controlled clinical trial is to evaluate whether an online Mindfulness-Based Intervention for Emotional Distress (MIED) can reduce emotional distress and reflux-related symptoms in adults with gastroesophageal reflux disease (GERD). GERD is a common chronic gastrointestinal condition that is frequently accompanied by anxiety, depressive symptoms,…

NCT07584096 — Effect of Inspiratory Muscle Training on Symptom Severity and Quality of Life in Non-Erosive Reflux Disease

StatusNot yet recruiting
PhaseN/A
SponsorIzmir University of Economics
Enrollment60
Study TypeINTERVENTIONAL
ConditionsNon-erosive Reflux Disease (NERD)
Interventions;

The goal of this clinical trial is to learn if inspiratory muscle training (IMT) works to treat on clinical symptom severity and quality of life in patients with Non-erosive reflux disease (NERD). The main questions it aims to answer are:

Does drug IMT lower the clinical symptom severity ? Does drug IMT improve quality of life? Researchers will compare high intensity IMT to a sham-IMT (a IMT d…

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.

NCT07651579 — Evaluation of the Impact of Periodontitis and Its Treatment on Swallowing Functions and Oral Quality of Life

StatusNot yet recruiting
PhaseN/A
SponsorUniversity Hospital, Clermont-Ferrand
Enrollment44
Study TypeINTERVENTIONAL
ConditionsPeriodontitis; Periodontal Diseases; Quality of Life
Interventions

The objective of this single-center prospective study is to evaluate the impact of periodontal treatment on masticatory performance in patients with periodontitis.

Participants will be asked to complete several questionnaires related to their oral health and quality of life. Functional masticatory tests and salivary flow measurements will also be performed.

NCT07659080 — Antireflux Surgery Without Preoperative Esophageal Manometry

StatusNot yet recruiting
PhaseN/A
SponsorMcMaster University
Enrollment96
Study TypeINTERVENTIONAL
ConditionsGERD; Hiatal Hernia; Heartburn; Paraesophageal Hernia; Gastroesophageal Reflux
Interventions;

The goal of this clinical trial is to learn if people can safely skip a test called esophageal manometry before surgery for acid reflux (gastroesophageal reflux disease, or GERD) or a hiatal hernia. Manometry measures the muscles of the food pipe using a thin tube passed through the nose. The test can be uncomfortable and can delay surgery. The main questions this study aims to answer are wheth…

NCT06579989 — Usefulness and Feasibility of Ultrasound in Office Laryngology Procedures

StatusNot yet recruiting
PhaseN/A
SponsorWeill Medical College of Cornell University
Enrollment200
Study TypeINTERVENTIONAL
ConditionsCough; Vocal Cord Atrophy; Vocal Cord Paresis; Vocal Cord Paralysis; Dysphagia
Interventions; ;

Investigators will assess the usefulness of using ultrasound in office procedures for laryngology interventions. Participants who qualify will be adults who are undergoing superior laryngeal nerve block, injection laryngoplasty, swallowing evaluation, voice evaluation and voice therapy.

NCT07659275 — Swallowing Assessment for Predicting Extubation Failure in Critically Ill Patients

StatusNot yet recruiting
PhaseN/A
SponsorUniversidade Federal de Pernambuco
Enrollment800
Study TypeOBSERVATIONAL
ConditionsExtubation Failure; Mechanical Ventilation; Critical Illness

Extubation failure, defined as the need for reintubation after planned removal of the endotracheal tube, occurs in up to 20% of critically ill patients and is associated with prolonged mechanical ventilation, longer intensive care unit (ICU) stay, and increased mortality. Current assessments of extubation readiness focus primarily on respiratory performance and do not routinely evaluate upper a…

NCT07654088 — AI-Enabled Mobile App for Safe Eating in Older Adults With Dysphagia

StatusNot yet recruiting
PhaseN/A
SponsorKAM Chi Shan Anna
Enrollment332
Study TypeINTERVENTIONAL
ConditionsDeglutition Disorders; Dysphagia
Interventions;

Difficulty swallowing (called dysphagia) is common in older adults and can make eating and drinking unsafe. It may lead to serious problems such as choking, lung infections, poor nutrition, and reduced quality of life. One common way to reduce these risks is to modify food and drink textures (for example, making foods softer or liquids thicker). However, people often find it difficult to prepar…

Enrolling by Invitation

NCT03103789 — Assessment of Esophageal Epithelium Integrity With Use of a Novel Mucosal Impedance Device

StatusEnrolling by invitation
PhaseN/A
SponsorVanderbilt University Medical Center
Enrollment75
Study TypeOBSERVATIONAL
ConditionsGastro Esophageal Reflux
Interventions;

The objective of this study is to design and use a novel, minimally invasive mucosal impedance (MI) technology to inexpensively and accurately test mucosal health in suspected gastroesophageal reflux disease (GERD) and nonerosive reflux disease (NERD) patients as compared to those without GERD.

Completed Trials

NCT03105375 — Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of X842 in Human: A Single/Multiple Ascending Dose Study

StatusCompleted
PhaseEarly Phase 1
SponsorCinclus Pharma Holding AB
Enrollment39
Study TypeINTERVENTIONAL
ConditionsHealthy Volunteers
Interventions; ;

The purpose of this study is to assess and analyze the safety, tolerability and PK/PD data following single ascending and multiple ascending doses of X842 in healthy subjects.

NCT03596411 — The Detection of Barrett’s Esophagus by Gastrointestinal Endoscopy Prevents Esophageal Carcinoma in Morbid Obese After Sleeve Gastrectomy

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nice
Enrollment100
Study TypeOBSERVATIONAL
ConditionsGastroesophageal Reflux

Severe Gastroesophageal reflux disease (GERD) leading to a chronic aggression of esophagus mucosa, called Barrett’s esophagus is a main complication of Sleeve gastrectomy for morbid obesity. Barrett’s esophagus is considered as a early stage of neoplastic transformation to adenocarcinoma. Since this last years, six european bariatric centers have adopted the policy to realize endoscopy before a…

NCT04402931 — Redo Surgery or Transcatheter Valve-in-Valve for Mitral Bioprosthetic Dysfunction (SURViV)

StatusCompleted
PhaseN/A
SponsorInstituto Dante Pazzanese de Cardiologia
Enrollment150
Study TypeINTERVENTIONAL
ConditionsMitral Prosthetic Valve Stenosis and Regurgitation
Interventions;

Transcatheter valve-in-valve implantation has emerged as a valid alternative to redo surgery for patients with surgical bioprosthetic dysfunction. Nowadays, transcatheter, transeptal mitral valve-in-valve replacement (TsMViV) has been adopted in many centers worldwide. Some studies report low rates of periprocedural morbidity and mortality and favorable hemodynamic parameters of valve performan…

NCT07400822 — Effect of Sour Taste on Swallowing Function of Patients With Dysphagia After Acute Ischemic Stroke

StatusCompleted
PhaseN/A
SponsorAYFER GUNES
Enrollment95
Study TypeINTERVENTIONAL
ConditionsDsyphagia After Stroke; Acute Cerebrovascular Accident
Interventions;

This randomized controlled study was designed to determine the Effect of Sour Taste on Swallowing Function of Patients with Dysphagia After Acute Ischemic Stroke The study was conducted between july 2021 and november 2022 with 95 patients diagnosed with Acute Ischemic Stroke (47 intervention, 48 control) at the neurology clinic and outpatient clinic of a university hospital in Edirne. Data were…

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…

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…

NCT06791590 — Evaluating the Effects of Intermittent Oro-esophageal in Tracheotomy Patients With Neurogenic Dysphagia

StatusCompleted
PhaseN/A
SponsorCapital Medical University
Enrollment140
Study TypeINTERVENTIONAL
ConditionsNeurogenic Dysphagia; Tracheotomy Patients
Interventions;

Neurogenic dysphagia refers to swallowing disorders caused by the damage of swallowing central or peripheral nerves and muscles. According to statistics, about 50% of patients with neurological diseases will be complicated with neurogenic dysphagia. Common diseases include stroke, dementia, Parkinson’s disease and neuromuscular diseases. Dysphagia has a great impact on the quality of life of pa…

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 …

NCT07658612 — Research on the Possible Relationship Between Sarcopenia and Oral Muscle Function

StatusCompleted
PhaseN/A
SponsorChang Gung University of Science and Technology
Enrollment251
Study TypeOBSERVATIONAL
ConditionsNon-sarcopenic Subjects; Possible Sarcopenia; Sarcopenia (With Low ASM by BIM)
Interventions

This study will focus on community-dwelling elderly individuals and will follow the community screening process recommended by AWGS.

It is expected to recruit 100 individuals who may have sarcopenia and 300 healthy or sub-healthy elderly individuals who are not likely to have sarcopenia, totaling 400 participants.Basic data such as age and body composition will be collected, as well as dietary…

NCT07379645 — A Clinical Trial of PepZinGI® for Acute Heartburn Relief and Sleep Outcomes

StatusCompleted
PhaseN/A
SponsorNutriScience Innovations, LLC
Enrollment50
Study TypeINTERVENTIONAL
ConditionsHeartburn
Interventions;

This decentralized, randomized, double-blind, placebo-controlled, two-period crossover study will evaluate whether PepZinGI® (zinc-L-carnosine) reduces food-triggered heartburn compared with placebo. Participants (N=50) complete two 1-week treatment periods (PepZinGI® and placebo) separated by a 2-week washout, for a total of 29 days. Primary outcomes are heartburn severity and frequency measur…

Other (Terminated)

NCT06317675 — Osteopathic Manipulative Treatment for Gastro-oesophageal Reflux Disease

StatusTerminated
PhasePhase 2
SponsorStudio Osteopatico Busto Arsizio
Enrollment26
Study TypeINTERVENTIONAL
ConditionsGastro-oesophageal Reflux Disease
Interventions

To evaluate the effects of osteopathic manipulative treatment in patients affected by symptoms related to gastro-oesophageal reflux disease (GERD)