Clinical Trials for Allergy

Currently registered clinical trials for Allergy from ClinicalTrials.gov. 25 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 Allergy from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 25
  • Active, not recruiting: 7
  • Completed: 10
  • Other: 8

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

Recruiting Trials

NCT00001532 — Role of Genetic Factors in the Development of Lung Disease

StatusRecruiting
PhaseN/A
SponsorNational Heart, Lung, and Blood Institute (NHLBI)
Enrollment3500
Study TypeOBSERVATIONAL
ConditionsCystic Fibrosis; Pulmonary Fibrosis; Tuberous Sclerosis; Asthma; Pulmonary Sarcoidosis

This study is designed to evaluate the genetics involved in the development of lung disease by surveying genes involved in the process of breathing and examining the genes in lung cells of patients with lung disease.

The study will focus on defining the distribution of abnormal genes responsible for processes directly involved in different diseases affecting the lungs of patients and healthy v…

NCT00605878 — Studies of Skin Microbes in Healthy People and in People With Skin Conditions

StatusRecruiting
PhaseN/A
SponsorNational Human Genome Research Institute (NHGRI)
Enrollment530
Study TypeOBSERVATIONAL
ConditionsEczema; Atopic Dermatitis

This study will examine microbes (e.g., bacteria, fungi, viruses) that live on human skin and how microbes contribute to health and disease. It will analyze healthy human skin and how the these microorganisms might change in patients with atopic dermatitis (AD), a skin condition also known as eczema.

Healthy volunteers, as well as patients with moderate to severe eczema (AD), between 2 and 40 …

NCT00341237 — Personalized Environment and Genes Study

StatusRecruiting
PhaseN/A
SponsorNational Institute of Environmental Health Sciences (NIEHS)
Enrollment25000
Study TypeOBSERVATIONAL
ConditionsDiabetes; Heart Disease; Asthma

Despite the overwhelming focus on genetic and genomic causes of human disease over the past two decades, it has been estimated that genetics is currently known to explain only 20% and 40% of the etiology of common disease. Thus, it is becoming increasingly apparent that human disease is a consequence of both genetic susceptibility and environmental exposures. Importantly, while individuals cann…

NCT01631617 — Effects of Treatments on Atopic Dermatitis

StatusRecruiting
PhasePhase 2
SponsorNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Enrollment130
Study TypeINTERVENTIONAL
ConditionsEczema; Dermatitis; Skin Diseases, Genetic; Dermatitis, Atopic; Skin Diseases
Interventions; ;

Background:

- Atopic dermatitis, or eczema, is a chronic skin disorder. Patients sometimes have infections with S. aureus bacteria. Researchers want to study how eczema treatments affect the number and the type of bacteria on the skin.

Objectives:

- To study the effect of eczema treatments on skin bacteria.

Eligibility:

  • Individuals between 2 and 25 years of age who have moderate to sev…

NCT03980886 — Characteristics and Inflammatory Markers in Children With Eosinophilic Esophagitis (EoE)

StatusRecruiting
PhaseN/A
SponsorUniversity of California, San Diego
Enrollment1500
Study TypeOBSERVATIONAL
ConditionsEosinophilic Esophagitis

Single center observational and specimen banking study for children with eosinophilic esophagitis EoE to gauge natural history and inflammatory markers

NCT05579366 — Rinatabart Sesutecan (Rina-S, PRO1184, GEN1184) for Advanced Solid Tumors (GCT1184-01/ PRO1184-001)

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorGenmab
Enrollment884
Study TypeINTERVENTIONAL
ConditionsHigh Grade Epithelial Ovarian Cancer; High Grade Serous Ovarian Cancer; Primary Peritoneal Carcinoma; Fallopian Tube Cancer; Endometrial Cancer
Interventions; ;

This study will test the safety, including side effects, and determine the characteristics of a drug called Rina-S in participants with solid tumors.

Participants will have solid tumor cancer that has spread through the body (metastatic) or cannot be removed with surgery (unresectable).

NCT05689151 — A Study to Learn About Abrocitinib in Adult Patients With Moderate to Severe Atopic Dermatitis.

StatusRecruiting
PhaseN/A
SponsorPfizer
Enrollment183
Study TypeOBSERVATIONAL
ConditionsAtopic Dermatitis; Eczema
Interventions

The purpose of this study is to learn about the safety and effects of Abrocitinib in the real-life clinical setting given for the treatment of moderate to severe atopic dermatitis. Atopic dermatitis, or AD, is a long-lasting disease that causes inflammation, redness, and irritation of the skin.

This study is seeking participant who are older than 18 years with moderate-to-severe chronic AD. Pa…

NCT05942300 — CPI-0209 Plus Carboplatin in Patients With Platinum Sensitive Recurrent Ovarian Cancer

StatusRecruiting
PhasePhase 1
SponsorLan Coffman
Enrollment30
Study TypeINTERVENTIONAL
ConditionsRecurrent Ovarian Cancer
Interventions;

This is a clinical trial using CPI-0209 in combination with Carboplatin chemotherapy followed by CPI-0209 maintenance in patients with platinum sensitive, recurrent ovarian cancer.

NCT06311682 — A Trial to Evaluate the Efficacy and Safety of Tralokinumab in Combination With Topical Corticosteroids in Children and Infants With Moderate-to-severe Atopic Dermatitis

StatusRecruiting
PhasePhase 3
SponsorLEO Pharma
Enrollment195
Study TypeINTERVENTIONAL
ConditionsAtopic Dermatitis
Interventions;

The purpose of this trial is to test whether treatment with tralokinumab (administered subcutaneous injections [SC]) in combination with topical corticosteroids (TCS) is safe and effective to treat moderate-to-severe atopic dermatitis (AD) in children and infants. This will be judged by a range of assessments that rate the severity and extent of atopic dermatitis and its symptoms, as well as …

NCT07005154 — A Phase 2 Study to Evaluate the Effects of ASP5541 in Participants With Prostate Cancer

StatusRecruiting
PhasePhase 2
SponsorAstellas Pharma Global Development, Inc.
Enrollment218
Study TypeINTERVENTIONAL
ConditionsProstate Cancer; Metastatic Castration-Resistant Prostate Cancer; Metastatic Hormone Sensitive Prostate Cancer
Interventions; ;

Hormone therapy, or androgen deprivation therapy (ADT) is a standard way to treat prostate cancer. It works by reducing the amount of the main male sex hormone, testosterone in the body. Androgen receptor pathway inhibitors (ARPIs) are another type of hormone therapy. They either slow down how much testosterone is made or block testosterone from reaching the prostate cancer cells. Abiraterone a…

NCT07690345 — Fungal Status and Prognosis in ABPA

StatusRecruiting
PhaseN/A
SponsorQianfoshan Hospital
Enrollment114
Study TypeOBSERVATIONAL
ConditionsABPA; Allergic Bronchopulmonary Aspergillosis; Allergic Bronchopulmonary Aspergillosis (ABPA); Colonization

This multicenter bidirectional cohort study aims to investigate the clinical characteristics and prognostic outcomes of patients with allergic bronchopulmonary aspergillosis (ABPA) stratified by fungal microbiological status in sputum or bronchoalveolar lavage fluid (BALF).

Patients diagnosed with ABPA according to the ISHAM 2024 criteria will be classified into fungal-positive and fungal-nega…

NCT07406282 — A Study to Learn About Real-world Utilization and Outcomes of Darolutamide and Other Androgen Receptor Pathway Inhibitors (ARPIs) for Newly Diagnosed Metastatic Hormone-sensitive Prostate Cancer (de Novo mHSPC) in US Urology Clinics

StatusRecruiting
PhaseN/A
SponsorBayer
Enrollment1400
Study TypeOBSERVATIONAL
ConditionsProstatic Neoplasms; Metastatic Hormone-Sensitive Prostate Cancer
Interventions; ;

Prostate cancer is the most common non-skin cancer among men in the United States. For some men, the cancer has already spread to other parts of the body at the time of diagnosis; this is called metastatic hormone-sensitive prostate cancer (mHSPC). Treatment for mHSPC has advanced significantly, with new standards of care involving androgen deprivation therapy (ADT) combined with drugs known as…

NCT07219173 — A Study to Evaluate Brenipatide Compared With Placebo in Adult Participants With Uncontrolled Moderate to Severe Asthma

StatusRecruiting
PhasePhase 2
SponsorEli Lilly and Company
Enrollment531
Study TypeINTERVENTIONAL
ConditionsAsthma
Interventions; ;

The purpose of this study is to assess the safety and efficacy of brenipatide at different dose levels compared with placebo in participants with moderate-to-severe asthma.

Study participation will last approximately 65 weeks, including screening, treatment, and follow-up periods.

NCT07213804 — A Three-Part Phase 3 Study of Sofetabart Mipitecan in Participants With Platinum-Resistant (Part A) and Platinum-Sensitive (Parts B and C) Ovarian Cancer

StatusRecruiting
PhasePhase 3
SponsorEli Lilly and Company
Enrollment1630
Study TypeINTERVENTIONAL
ConditionsOvarian Neoplasms; Fallopian Tube Neoplasms; Peritoneal Neoplasms; Neoplasm Metastasis
Interventions; ;

This is a clinical study that has three parts. It is testing a potential new medicine called Sofetabart Mipitecan (Sofe-M) for people with certain types of ovarian, peritoneal, and fallopian tube cancers. Part A enrolls participants with platinum-resistant cancer, meaning their disease progressed during or within six months of platinum-based chemotherapy. Parts B and C enroll participants with …

NCT07288138 — A Study of a Thyroid Hormone Receptor Beta Isoform (THRβ) Agonist and an Semicarbazide Sensitive Amine Oxidase (SSAO) Inhibitor, Alone and in Combination, in Adults With Presumed Metabolic Dysfunction-associated Steatohepatitis (MASH)

StatusRecruiting
PhasePhase 2
SponsorEccogene
Enrollment160
Study TypeINTERVENTIONAL
ConditionsMetabolic Dysfunction-associated Steatohepatitis
Interventions; ;

The primary objective of this trial is to evaluate the dose-dependent and comparative effects of ECC4703 (low and high dose), ECC0509 (low and high dose), and their combination on hepatic fat reduction as assessed by change in magnetic resonance imaging proton density fat fraction (MRI-PDFF) at Week 12.

NCT07602192 — Quantitative Chest CT and Multi-Omics to Distinguish Asthma From COPD and Predict Treatment Response

StatusRecruiting
PhaseN/A
SponsorKorea University Guro Hospital
Enrollment200
Study TypeOBSERVATIONAL
ConditionsAsthma (Diagnosis); COPD (Chronic Obstructive Pulmonary Disease)

This study aims to improve the diagnosis and treatment prediction of asthma and chronic obstructive pulmonary disease (COPD) by combining quantitative chest computed tomography (CT) imaging with multi-omics data.

Adults with asthma or COPD will be enrolled and undergo routine clinical evaluations, pulmonary function tests, blood tests, and chest CT scans. Additional samples, such as sputum and…

NCT07223697 — A Long Term Extension Study to Evaluate the Safety and Efficacy of Afimkibart (RO7790121) in Participants With Atopic Dermatitis

StatusRecruiting
PhasePhase 2
SponsorHoffmann-La Roche
Enrollment120
Study TypeINTERVENTIONAL
ConditionsAtopic Dermatitis
Interventions

This study will assess long-term safety and efficacy of Afimkibart (also known as RO7790121) in participants with Atopic Dermatitis (AD) who participated in previous afimkibart clinical trials.

NCT07605078 — Associations Between Household Mold Levels and Physical and Mental Health: A Mold and Mycotoxin Testing Research Registry

StatusRecruiting
PhaseN/A
SponsorOvationLab
Enrollment2500
Study TypeOBSERVATIONAL
ConditionsMold Illness; Mold or Dust Allergy
Interventions

The primary purpose of this study is to evaluate cross-sectional associations between mold exposures identified with The Dust Test and self-reported physical health, emotional health, and medical diagnoses. In addition, associations between mold exposures and mycotoxin levels among users who have done mycotoxin lab testing will also be evaluated.

NCT07592585 — Phase III Clinical Study of VC005 in Adult and Adolescents With Mild to Moderate Atopic Dermatitis

StatusRecruiting
PhasePhase 3
SponsorJiangsu vcare pharmaceutical technology co., LTD
Enrollment360
Study TypeINTERVENTIONAL
ConditionsAtopic Dermatitis
Interventions;

A multicenter, randomized, double-blind, vehicle controlled phase III clinical study to evaluate the efficacy and safety of VC005 in adults and adolescents with mild to moderate atopic dermatitis

NCT07687524 — LOVING (Learning About Our Behavior is Valuable for Increasing Nurturing Relationships and Healthy Growth) RCT

StatusRecruiting
PhaseN/A
SponsorNational University of Singapore
Enrollment624
Study TypeINTERVENTIONAL
ConditionsChild Development; Child Behavioral Problems; Parent Child Relationship
Interventions; ;

The LOVING study is a randomized controlled trial designed to determine whether adaptations to an internationally recognized parenting program that enhances sensitive caregiving likewise improves sensitive caregiving in Singapore and, in turn, downstream child outcomes in emotional, behavioral, and cognitive development during the early childhood years.

Research shows that sensitive caregiving…

NCT07598383 — A Multicenter, Randomized, Double-blind, Vehicle Controlled Phase II Clinical Study to Evaluate the Efficacy and Safety of VC005 Gel in Adult Subjects With Mild to Moderate Atopic Dermatitis

StatusRecruiting
PhasePhase 2
SponsorJiangsu vcare pharmaceutical technology co., LTD
Enrollment120
Study TypeINTERVENTIONAL
ConditionsAtopic Dermatitis
Interventions;

This is a multicenter, randomized, double-blind, vehicle controlled phase II clinical study to evaluate the efficacy and safety of VC005 gel in adult subjects with mild to moderate atopic dermatitis

NCT07619820 — A Phase 1b Study to Evaluate the PK of CSL300 (Clazakizumab) in Chinese Subjects With End Stage Kidney Disease (ESKD)

StatusRecruiting
PhasePhase 1
SponsorCSL Behring
Enrollment24
Study TypeINTERVENTIONAL
ConditionsEnd Stage Kidney Disease (ESKD)
Interventions;

This is a phase 1b, partial-blind (Sponsor unblinded), randomized, multicenter, placebo-controlled study. The primary objective of this study is to evaluate the pharmacokinetics (PK) of CSL300 after single and multiple doses in Chinese participants with end stage kidney disease (ESKD) undergoing dialysis.

NCT07546981 — Efficacy and Safety of CHF 5993 100/6/12.5 μg HFA-152a pMDI in Patients With Asthma Uncontrolled on Medium Doses of Inhaled Corticosteroids in Combination With Long-acting ß2-agonists

StatusRecruiting
PhasePhase 3
SponsorChiesi Farmaceutici S.p.A.
Enrollment554
Study TypeINTERVENTIONAL
ConditionsAsthma
Interventions;

This is a study comparing CHF 5993 pMDI HFA-152a with CHF 1535 pMDI HFA-134a in Chinese patients with asthma uncontrolled on medium doses of ICS+LABA.

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…

NCT07262983 — Evaluating the Safety and Tolerability of Baricitinib in Patients With Job Syndrome With Lupus-Like Disease and/or Atopic Dermatitis

StatusRecruiting
PhasePhase 1
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment20
Study TypeINTERVENTIONAL
ConditionsHyper IgE Syndrome From STAT3 Mutation; Job s Syndrome; HIES; Lupus; Atopic Dermatitis
Interventions

Background:

Autosomal dominant hyper-IgE syndrome (HIES), also called Job syndrome, is a genetic disorder that affects the immune system. It can cause skin and lung infections and problems with blood vessels, connective tissues, and bones. People with HIES often have lupus-like disease or atopic dermatitis (skin rash). Researchers want to know if a drug approved to treat other immune system di…

Active, Not Recruiting

NCT00719719 — Cause of Unexplained Anaphylaxis

StatusActive, not recruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment115
Study TypeOBSERVATIONAL
ConditionsIdiopathic Anaphylaxis; Drug Anaphylaxis; Venom Anaphylaxis; Food Anaphylaxis

This study will explore the possible cause of unexplained, or idiopathic, anaphylaxis. Anaphylaxis is a rapid, life-threatening, severe reaction that occurs suddenly after contact with an allergy-causing substance, usually a particular food, drug or stinging insect. The allergen triggers mast cells to release several substances, including histamine. Histamine is responsible for many of the symp…

NCT01759186 — Airway Redox and Gender Determinants in Severe Asthma

StatusActive, not recruiting
PhaseN/A
SponsorThe Cleveland Clinic
Enrollment300
Study TypeOBSERVATIONAL
ConditionsAsthma

The investigators will study the biologic and chemical differences that cause the greater incidence, and severity of asthma in women as compared to men. Severe asthma affects boys more than girls, while severe asthma in adults is predominantly a disease of women. The investigators aim to identify the processes that occur in the body that are behind the onset of severe asthma in young women duri…

NCT05794906 — A Study to Compare Darolutamide Given With Androgen Deprivation Therapy (ADT) and Placebo Given With ADT in Men With Hormone Sensitive Prostate Cancer and Raise of Prostate Specific Antigen (PSA) Levels After Local Therapies

StatusActive, not recruiting
PhasePhase 3
SponsorBayer
Enrollment985
Study TypeINTERVENTIONAL
ConditionsBiochemically Recurrent Prostate Cancer
Interventions; ;

Researchers are looking for a better way to treat men at high-risk of biochemical recurrence (BCR) of prostate cancer.

BCR means that in men who had prostate cancer and were treated by either surgery and/ or radiation therapy, the blood level of a specific protein called PSA rises. PSA is a marker of prostate cancer cells activity. The PSA increase means that the cancer has come back even thou…

NCT05851443 — A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Inadequately Controlled Moderate to Severe Asthma

StatusActive, not recruiting
PhasePhase 2
SponsorIncyte Corporation
Enrollment247
Study TypeINTERVENTIONAL
ConditionsModerate to Severe Asthma
Interventions; ;

The study is being conducted to evaluate the effect of 3 dosing regimens of povorcitinib on pulmonary function

NCT06874114 — An Observational Study to Learn More About Treatment Patterns and Factors Determining the Choice of Treatment in Canadian Men With Metastatic Hormone Sensitive Prostate Cancer in Routine Medical Care

StatusActive, not recruiting
PhaseN/A
SponsorBayer
Enrollment700
Study TypeOBSERVATIONAL
ConditionsMetastatic Hormone-sensitive Prostate Cancer

This is an observational study in which only data are collected from adult Canadian men with metastatic hormone sensitive prostate cancer (mHSPC) are studied. Participants will not receive any advice on treatment or any changes to the healthcare.

Metastatic hormone sensitive prostate cancer is a cancer of the prostate gland, a male reproductive gland found below the bladder. Metastatic means t…

NCT06853626 — One-hoUr Troponin Using a High-sensitivity Point-Of-Care Assay in Emergency Primary Care

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Oslo
Enrollment2500
Study TypeINTERVENTIONAL
ConditionsAcute Myocardial Infarction (AMI); Chest Pain; Acute Coronary Syndromes (ACS); Non-cardiac Chest Pain; Troponin
Interventions

Acute chest pain is a prevalent medical emergency in primary emergency care settings. Triage of chest pain prior to hospital admission presents significant challenges due to the absence of sufficiently sensitive diagnostic tools. Clinical signs, symptoms, risk assessment scores, or a normal electrocardiogram (ECG) can reliably exclude acute myocardial infarction (MI). This diagnostic uncertaint…

NCT07344779 — A Study to Learn How Men With Advanced Prostate Cancer Respond to Treatment With Darolutamide and Hormone Therapy, With or Without Chemotherapy, in Real-world Medical Practice

StatusActive, not recruiting
PhaseN/A
SponsorBayer
Enrollment1600
Study TypeOBSERVATIONAL
ConditionsMetastatic Hormone-Sensitive Prostate Cancer
Interventions; ;

This is an international, prospective, open-label, multicenter, multi-cohort, non-interventional observational study designed to describe the real-world effectiveness and safety of darolutamide in combination with androgen deprivation therapy (ADT), with or without docetaxel, in patients with metastatic hormone-sensitive prostate cancer (mHSPC). The study aims to enroll approximately 1,600 male…

Not Yet Recruiting

NCT07688772 — A Clinical Study Evaluating the Efficacy and Safety of SHR-1819 Injection in Patients With Seasonal Allergic Rhinitis

StatusNot yet recruiting
PhasePhase 3
SponsorGuangdong Hengrui Pharmaceutical Co., Ltd
Enrollment196
Study TypeINTERVENTIONAL
ConditionsSeasonal Allergic Rhinitis
Interventions;

This study is a multicenter, randomized, double-blind, placebo-controlled Phase III clinical trial aimed at evaluating the efficacy, safety, pharmacokinetics (PK), pharmacodynamics (PD), and immunogenicity of SHR-1819 injection in patients with Seasonal Allergic Rhinitis (SAR).

NCT07564141 — Study to Assess the Efficacy and Safety of Rina-S With or Without Bevacizumab Compared to Investigator’s Choice of Platinum-based Chemotherapy With or Without Bevacizumab as Second-line Treatment in Participants With Recurrent Platinum-sensitive Ovarian Cancer

StatusNot yet recruiting
PhasePhase 3
SponsorGenmab
Enrollment688
Study TypeINTERVENTIONAL
ConditionsPlatinum-Sensitive Ovarian Cancer; Ovarian Cancer
Interventions; ;

This Phase 3 study will be conducted in different countries around the world with up to about 688 participants.

The purpose of this study is to evaluate how well Rina-S works against ovarian cancer in combination with or without bevacizumab and how it compares to an investigator’s choice of platinum-based chemotherapy with or without bevacizumab.

Participants will receive either:

  • Rina-S mo…

NCT07654842 — Fasenra: An Asthma Study

StatusNot yet recruiting
PhasePhase 4
SponsorEndeavor Health
Enrollment40
Study TypeINTERVENTIONAL
ConditionsEosinophilic Asthma; Severe Asthma; Severe Eosinophilic Asthma; Asthma
Interventions;

The goal of this observational study is to learn more about the effectiveness of benralizumab (Fasenra, 30 mg every 8 weeks) in maintaining asthma control in people with severe eosinophilic asthma.

Participants will have electronic medication monitors fitted to their usual maintenance inhaler, as well as a study-provided anti-inflammatory rescue inhaler, albuterol-budesonide (AirSupra). These …

NCT05713799 — Trial of the Combination of Alpha-Lipoic Acid and Mirabegron in Women and in Men With Obesity

StatusNot yet recruiting
PhasePhase 2
SponsorNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Enrollment60
Study TypeINTERVENTIONAL
ConditionsInsulin Resistance; Obesity
Interventions; ;

Background:

Obesity and related illnesses cause at least 2.8 million deaths each year worldwide. Few treatments exist for obesity that are safe and widely available. A study drug (mirabegron [MG]) combined with a supplement (alpha-lipoic acid [ALA]) may help.

Objective:

To learn how MG and ALA can help the body process food.

Eligibility:

People aged 18 to 65 years with a body mass inde…

NCT06960759 — Mechanisms of Change in Behavioral Cough Suppression Therapy for Refractory Chronic Cough

StatusNot yet recruiting
PhasePhase 2
SponsorUniversity of Montana
Enrollment135
Study TypeINTERVENTIONAL
ConditionsChronic Cough (CC); Refractory Chronic Cough; Unexplained Chronic Cough
Interventions;

This study is testing new ways to help people who have chronic cough that has not improved with typical treatments. One approach is called behavioral cough suppression (BCS) therapy, which teaches people techniques to stop themselves from coughing. Another approach uses a natural substance thought to help reduce the body’s sensitivity to cough triggers.

In this study, we will test two treatmen…

NCT07686484 — A Trial of HRS-3095 in Healthy Volunteers

StatusNot yet recruiting
PhaseEarly Phase 1
SponsorAtridia Pty Ltd.
Enrollment36
Study TypeINTERVENTIONAL
ConditionsChronic Spontaneous Urticaria
Interventions; ;

The purpose of this study is to assess safety, PK, Pharmacodynamic profile of a single dose of HRS-3095 in healthy participants

NCT07687797 — Partially Hydrolysed Whey Based Formula in Differentiation Between Non IgE Gastrointestinal Cow’s Milk Protein Allergy and Milk Intolerance

StatusNot yet recruiting
PhaseN/A
SponsorAin Shams University
Enrollment100
Study TypeINTERVENTIONAL
ConditionsCow Milk Protein Allergy; Cow Milk Intolerance
Interventions;

Partially hydrolysed whey based formula in differentiation between non IgE gastrointestinal cow’s milk protein allergy and milk intolerance

NCT07504588 — Sacituzumab Govitecan With Bevacizumab Compared to Usual Chemotherapy (Carboplatin, Pegylated Liposomal Doxorubicin and Bevacizumab) for Treating Recurrent Platinum-Sensitive Ovarian Cancer After PARP Inhibitor Maintenance Therapy

StatusNot yet recruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment87
Study TypeINTERVENTIONAL
ConditionsRecurrent Platinum-Sensitive Fallopian Tube Endometrioid Adenocarcinoma; Recurrent Platinum-Sensitive Fallopian Tube High Grade Serous Adenocarcinoma; Recurrent Platinum-Sensitive Ovarian High Grade Endometrioid Adenocarcinoma; Recurrent Platinum-Sensitive Ovarian High Grade Serous Adenocarcinoma; Recurrent Platinum-Sensitive Primary Peritoneal Endometrioid Adenocarcinoma
Interventions; ;

This phase II trial compares the effect of sacituzumab govitecan and bevacizumab to standard care (carboplatin, pegylated liposomal doxorubicin, and bevacizumab) in patients with ovarian cancer that has come back after an initial response to platinum therapy (platinum-sensitive), that has progressed after poly (adenosine diphosphate-ribose) polymerase (PARP) inhibitor maintenance therapy (recur…

Completed Trials

NCT00001888 — Sample Collections From the Airways of Asthmatic Patients

StatusCompleted
PhaseN/A
SponsorNational Heart, Lung, and Blood Institute (NHLBI)
Enrollment574
Study TypeOBSERVATIONAL
ConditionsAsthma

Fiberoptic bronchoscopy is a procedure which involves passing a pencil-thin tube into the lung in order to collect fluid and cells from the airways. Fiberoptic bronchoscopy can collect cells from the walls of airways by gently brushing them (bronchial brushing). In addition, squirting small amounts of sterile water in to the airway and gently suctioning it back into the bronchoscope (bronchoalv…

NCT01164241 — Natural History of Severe Allergic Inflammation and Reactions

StatusCompleted
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment945
Study TypeOBSERVATIONAL
ConditionsPGM3 Deficiency; Eosinophilic and/or Atopic Dermatitis; OSMR Deficiency; Primary Localized Cutaneous Amyloidosis; Hereditary Alpha-tryptasemia

Background:

- Allergic inflammation is central to allergy-related diseases and disorders, such as asthma, food allergies, and atopic dermatitis. Atopic dermatitis, commonly called eczema is a chronic, noncontagious skin condition, usually starting in the first years of life, which causes itching and scaling of an individual s skin. Because atopic dermatitis is a common condition in children w…

NCT00852943 — Screening Protocol for Genetic Diseases of Allergic Inflammation

StatusCompleted
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment824
Study TypeOBSERVATIONAL
ConditionsEosinophilic Disease; Immune Deficiency; HaTS; Urticaria Anaphylaxis; Elevated IgE Level

Background:

  • Mast cells are responsible for most symptoms of allergic reactions. In some allergic diseases, it is unusually easy to cause mast cells to release their contents and cause allergic reactions. In other cases, mast cells grow abnormally and, in rare cases, can result in tumors. Mast cells also control other parts of the immune system.
  • Understanding why mast cells behave abnormall…

NCT02745613 — Type 2 Diabetes Affect Exercise Induced Improvement in Insulin Sensitivity

StatusCompleted
PhaseN/A
SponsorUniversity of Texas, El Paso
Enrollment50
Study TypeINTERVENTIONAL
ConditionsInsulin Sensitivity/Resistance
Interventions

This study investigates whether: (i) a family history of type 2 diabetes affects exercise induced improvements in insulin sensitivity. (ii) being prediabetic affects exercise induced improvements in glycemic control. (iii) sex differences affect exercise induced improvements in glycemic control.

NCT03152669 — The Extended Salford Lung Study (“Ex-SLS”) Data Access Project

StatusCompleted
PhaseN/A
SponsorGlaxoSmithKline
Enrollment1183
Study TypeOBSERVATIONAL
ConditionsAsthma

The Salford Lung Study (SLS) subjects represent a group of COPD and asthma patients whose disease is extremely well-characterised over a short time period. Subjects in the SLS originally consented for information relevant to the study to be shared with the sponsor (GSK). These data were limited to three years prior to randomisation and the twelve-month interventional treatment period. Broadened…

NCT07687251 — Impact of Primary Nursing on Nursing-sensitive Outcomes in Inpatients Units: a Multicentre Pre-Post Study

StatusCompleted
PhaseN/A
SponsorUniversità degli Studi del Piemonte Orientale Amedeo Avogadro
Enrollment1708
Study TypeINTERVENTIONAL
ConditionsAccidental Falls; Cross Infection (Hospital-Acquired Infections); Acute Care Unit
Interventions

The aim of this quasi-experimental before-after study is to evaluate whether the implementation of the Primary Nursing (PN) pattern of care improves nursing-sensitive outcomes in adult inpatients and nurse-related outcomes across hospital wards in Northern Italy.

The main questions it aims to answer are:

  1. What is the impact of the PN on inpatients’ nursing-sensitive outcomes, including heal…

NCT04792697 — Experimental Manipulation of Sleep and Circadian Rhythms and the Role Played on Reward Function in Teens

StatusCompleted
PhaseN/A
SponsorUniversity of Pittsburgh
Enrollment115
Study TypeINTERVENTIONAL
ConditionsDelayed Sleep Phase Syndrome
Interventions; ;

Adolescence is a time of heightened reward sensitivity and greater impulsivity. On top of this, many teenagers experience chronic sleep deprivation and misalignment of their circadian rhythms due to biological shifts in their sleep/wake patterns paired with early school start times. Many studies find that this increases the risk for substance use (SU). However, what impact circadian rhythm and …

NCT04258332 — CARDIA-Salt Sensitivity of Blood Pressure (SSBP)

StatusCompleted
PhaseN/A
SponsorVanderbilt University Medical Center
Enrollment281
Study TypeINTERVENTIONAL
ConditionsSalt Sensitivity of Blood Pressure; Hypertension
Interventions;

Salt sensitivity of blood pressure (SSBP) is defined as the change in blood pressure (BP) in relation to change in salt intake. An increase in BP from low- to high-salt diet is common and associated with an increased risk of cardiovascular morbidity and mortality, even among normotensive individuals. Yet, the pathophysiology of SSBP is not well understood. The prevailing paradigm is that abnorm…

NCT05509569 — A Survey of Icatibant in Pediatric Participants With Hereditary Angioedema

StatusCompleted
PhaseN/A
SponsorTakeda
Enrollment32
Study TypeOBSERVATIONAL
ConditionsHereditary Angioedema (HAE)
Interventions

This study is a survey in Japan of Icatibant subcutaneous injection 30 mg syringe used to treat children or teenagers with acute attacks of hereditary angioedema (HAE). The study sponsor will not be involved in how the participants are treated but will provide instructions on how the clinics will record what happens during the study.

The main aim of the study is to check for side effects relat…

NCT06501274 — Capsule Sponge Study in Eosinophilic Oesophagitis

StatusCompleted
PhaseN/A
SponsorEast and North Hertfordshire NHS Trust
Enrollment143
Study TypeINTERVENTIONAL
ConditionsEosinophilic Esophagitis
Interventions

Open pragmatic, descriptive single site study in adult patients with non-stenotic eosinophilic oesophagitis.

To assess the clinical value of Capsule sponge in the assessment of treatment response in patients with known non-stenosing eosinophilic oesophagitis, as an alternative to gastroscopy in a real world setting.

To assess patient preference for Capsule sponge or gastroscopy. All patients …