Gastro-oesophageal Reflux Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have had ongoing acid reflux symptoms — such as heartburn or regurgitation — at least twice a week for the past 6 months
- People who have had a special acidity test (called an ambulatory pH study) that has confirmed acid reflux is occurring
Who may not be able to join:
- People who are unwilling or unable to participate or give their consent to join the trial
- People younger than 18 years old or older than 80 years old
- People who are allergic to or cannot tolerate medications called PPIs (proton pump inhibitors, a common type of acid reflux medication)
- People who have a large hiatal hernia (where part of the stomach pushes up into the chest) measuring more than 3 cm, with a specific severity grading (confirm with trial site)
- People who have Barrett's oesophagus (a condition where the lining of the food pipe is changed by long-term acid damage)
- People who have a narrowing of the food pipe that has previously required treatment
- People who have a serious disorder affecting the movement of food through their digestive system
- People who have a condition called eosinophilic oesophagitis (inflammation of the food pipe caused by a type of white blood cell)
- People who have been diagnosed with delayed stomach emptying (gastroparesis), confirmed by a gastric emptying test
- People who have previously had surgery on the stomach or food pipe, including fundoplication, myotomy, or LINX device placement
- People who have severe liver scarring (cirrhosis) along with enlarged veins in the food pipe or stomach (varices)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Prateek Sharma, MD, Kansas City VA Hospital
Phone: 816-861-4700
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in GERD health related quality of life (GERD-HRQL) score
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.