Phase 4 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:
- Adults aged 19 years or older who are Korean residents, as of the date of signing consent
- People who have been diagnosed with erosive gastroesophageal reflux disease (a condition where stomach acid damages the lining of the food pipe) confirmed by a camera examination of the upper digestive tract
- People who have experienced heartburn at night for more than 3 months at the time of their first screening visit
- People who have made a voluntary decision to take part and have signed a written consent form
Who may not be able to join:
- People who are unable to undergo a camera examination of the upper digestive tract
- People with a history of drug or alcohol misuse within the past year
- People who have taken part in another clinical trial and received an investigational product within one month before the screening visit
- People who have other health findings that the trial doctor considers medically unsuitable for this study (confirm with trial site)
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
Phone: +82-1544-9004
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
Proportion of participants without sleep disturbance related to nighttime heartburn during the last 7 days
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.