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Study identifier: NCT06613438 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: GERD (Gastroesophageal Reflux Disease)  ·  Sponsor: Gerd Care Medical Ltd

PhaseNA
Planned participants84
Who can joinAll sexes, 22 Years to 75 Years
Healthy volunteersNo

About this study

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 participants have when using the eGERD device? To assess the acidity in the esophagus, a wireless standard-of-care capsule called Bravo will be placed in the participants esophagus (throat) for several days. To assess GERD symptoms, participants will be requested to report symptoms they experience using a smartphone application. Researchers will compare a real version of the eGERD device to a sham version (a look-alike device that has no therapeutic effect) to see if the eGERD device is effective in treating GERD.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (5)

Division of Gastroenterology & Hepatology Feinberg School of Medicine Northwestern UniversityChicago, Illinois, United StatesNot Yet Recruiting
Gastroenterology department, Emek medical center (EMC)Afula, IsraelRecruiting
Gastroenterology department, Rambam Health Care CampusHaifa, IsraelRecruiting
Gastroenterology department, Rabin medical center (RMC)Petah Tikva, IsraelRecruiting
Gastroenterology department, Tel Aviv Sourasky Medical Center (Ichilov)Tel Aviv, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT06613438