Diet change may soothe stubborn heartburn when pills fail
NCT ID NCT02471989
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a low-FODMAP diet could help people with gastro-esophageal reflux disease (GERD) whose symptoms persist despite taking standard acid-reducing drugs (PPIs). Thirty-one adults with confirmed reflux were randomly assigned to either a low-FODMAP diet or a standard GERD diet for several weeks. The main goal was to see if the low-FODMAP diet led to more people achieving symptom remission, measured by a reflux symptom questionnaire.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Low-FODMAP diet
- What this could lead to
- If it works, this could offer a dietary approach to ease reflux symptoms for people whose GERD doesn't respond to standard acid-reducing medications.
- What could go wrong
- This was a small, early study with only 31 participants. Dietary changes can be hard to maintain, and results may not apply to everyone with GERD.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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31 people
The number who actually took part.
- Started
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Jan 2016
- Finished
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Nov 2018
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age \> 18 * Affiliation to French Social Security * Informed written consent * RDQ score \> 3 * Abnormal pH-impedance monitoring on PPI twice daily (since 3 months) according to normal values published by Zerbib et al (CGH 2013) Exclusion Criteria: * Pregnancy or breast feeding * Women of childbearing potential without an effective method of contraception * Person under guardianship * History of thoracic of abdominal surgery (excepted appendectomy and cholecystectomy)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Explorations fonctionnelles
Lyon, 69437, France
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Explorations fonctionnelles Digestives
Rennes, 35033, France
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Gastroentérologie
Colombes, 92700, France
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Gastroentérologie
Nantes, 44093, France
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Gastroentérologie
Rouen, 76031, France
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Hépato-Gastroentérologie et oncologie digestive,
Bordeaux, 33075, France