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Esophagitis clinical trials

View clinical trials related to Esophagitis.

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NCT ID: NCT05890001 Enrolling by invitation - Erosive Esophagitis Clinical Trials

A Study to Evaluate the Long-Term Safety of BLI5100 in Patients With Gastroesophageal Reflux Disease

Start date: April 5, 2023
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the safety of up to 12 months (52 weeks) of once daily oral administration of BLI5100 in patients with non-erosive reflux disease (NERD) or healed erosive esophagitis (EE).

NCT ID: NCT05813561 Completed - Reflux Esophagitis Clinical Trials

The Efficacy and Safety of DWP14012 in Chinese Patients With Reflux Esophagitis

Start date: December 30, 2021
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy, safety, and cost-effectiveness of DWP14012 40 mg compared to esomeprazole magnesium enteric-coated tablets for the treatment of reflux esophagitis.

NCT ID: NCT05774184 Recruiting - Clinical trials for Eosinophilic Esophagitis

A Study of CDX-0159 in Patients With Eosinophilic Esophagitis

EvolvE
Start date: June 1, 2023
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of barzolvolimab in adult Eosinophilic Esophagitis patients.

NCT ID: NCT05757856 Recruiting - Clinical trials for Eosinophilic Esophagitis

A Study to Investigate Safety and Tolerability of NDX-3315 and NDX-3324 in Healthy Participants and Patients With Eosinophilic Esophagitis

Start date: January 20, 2023
Phase: Phase 1
Study type: Interventional

An open-label phase 1b study to assess the safety and exploratory diagnostic performance of the oral radiopharmaceutical agent NDX-3315 and NDX-3324 in healthy participants and patients with eosinophilic esophagitis (EoE).

NCT ID: NCT05755477 Recruiting - Clinical trials for Eosinophilic Esophagitis

Survey About the Relationship Beetween Allergic Rhinitis and Seasonal EOE Exacerbations

Start date: January 3, 2021
Phase:
Study type: Observational

Eosinophilic esophagitis (EoE) is a chronic inflammatory esophagus disease that is presented in patients with a history of recurrent dysphagia. EoE is closely related to other pathologies with an immuno-allergic etiopathogenesis such as atopic dermatitis (AD), IgE-mediated food allergy, allergic rhinitis and bronchial asthma. While the importance of the correlation between diet and food allergy has been largely demonstrated, less is known about the exact role of sensitization to aerollergens in the progression and recrudescence of symptoms. In support of this correlation there is evidence of a seasonal trend in the new diagnoses of EoE, of the possibility of the de-novo onset of the pathology following massive exposure to a specific aeroallergen and the demonstration that the degree of esophageal eosinophilia varies according to the climatic zone and the season of the year. The detailed knowledge of this correlation could clarify some aspects of the etiopathogenesis and natural history of EoE, improve and personalize the clinical-diagnostic management of affected patients and provide new therapeutic targets. Our aim is evaluating the possible existence of a correlation between the recrudescence of dysphagia symptoms and a specific month of the year and/or specific season.

NCT ID: NCT05745857 Not yet recruiting - Clinical trials for Esophageal Adenocarcinoma

Oral Bevacizumab-800CW and Cetuximab-800CW Administration to Detect Early Esophageal Adenocarcinomas

SLURP
Start date: May 2023
Phase: Phase 2
Study type: Interventional

Previous studies have confirmed the great potential of quantitative fluorescence molecular endoscopy (qFME) when looking at additional lesion detection initially missed by high-definition white light endoscopy (HD-WLE) for surveillance of Barrett's esophagus.

NCT ID: NCT05730933 Recruiting - Clinical trials for Eosinophilic Esophagitis

An Intervention Study to Improve Therapeutic Compliance in Adult Patients With Eosinophilic Esophagitis.

Start date: April 12, 2023
Phase: N/A
Study type: Interventional

In many chronic conditions adherence to long-term treatment is a challenge, also for patients with eosinophilic esophagitis. Interventions, such as behavioral, educational and reminder interventions might improve treatment adherence. With this trial the investigators want to assess the effects of additional education in combination with more frequent follow up and patient reminders on adherence to treatment in adult patients with eosinophilic esophagitis.

NCT ID: NCT05695456 Recruiting - Clinical trials for Eosinophilic Esophagitis

Targeted Elimination Diet in EoE Patients Following Identification of Trigger Nutrients Using Confocal Laser Endomicroscopy

CLE-EoE
Start date: February 16, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

Using confocal laser endomicroscopy (CLE), gastrointestinal allergic reactions to certain foods in the duodenum will be evaluated on a cellular level. After that, a personalized exclusion diet will be followed based on the CLE results for 6 weeks, sham-controlled, in a cross-over fashion. Gastroscopy with esophageal biopsies will be repeated after each diet.

NCT ID: NCT05659576 Recruiting - Clinical trials for Radiation Esophagitis

Reducing Acute Upper Gastrointestinal Side-Effects of Thoracic Irradiation

Start date: December 13, 2022
Phase: Phase 2
Study type: Interventional

The purpose of the study is to explore options for preventing and reducing symptoms of radiation esophagitis (RE). The researchers will also look what symptoms participants experience, and whether there are differences in weight loss in participants.

NCT ID: NCT05634746 Active, not recruiting - Clinical trials for Eosinophilic Esophagitis

24-Week Induction Study of APT-1011 in Adult Subjects With Eosinophilic Esophagitis (EoE) (FLUTE 3)

Start date: December 29, 2022
Phase: Phase 3
Study type: Interventional

This is a 24-week randomized, double-blind, placebo-controlled induction study of APT-1011 in adults (≥18 years old) with eosinophilic esophagitis (EoE) followed by a single-arm, open-label extension. This study will evaluate the efficacy and safety of APT-1011 3 mg administered HS (hora somni, at bedtime) for the induction of response to treatment (symptomatic and histologic) over 24 weeks. The open-label extension will continue to evaluate long-term safety in subjects who consent to continue on open-label treatment with APT-1011.