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 are able to sign and date a consent form.
- People who are willing to follow all study procedures and are available for the whole duration of the study.
- People who have 3 or more established risk factors for Barrett's Oesophagus (a condition affecting the food pipe), which include: being over 50 years old, having long-term acid reflux, being male, being white, being a smoker, being obese, or having a family history of Barrett's Oesophagus or a related cancer called oesophageal adenocarcinoma.
Who may not be able to join:
- People who are not able to give their own consent to participate.
- People who have already been diagnosed with Barrett's Oesophagus or oesophageal adenocarcinoma.
- People who have a serious or life-limiting illness or disability.
- People who have active dementia or significant difficulties with memory and thinking.
- People who are currently incarcerated.
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: Sachin Wani, MD, University of Colorado, Denver
Phone: 303-724-0432
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
Define patient preferred BE/EAC screening test and barriers for attributes of BE/EAC screening tests
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.