New study tests antacid for Post-PPI acid rebound relief
NCT ID NCT07291700
First seen Jun 27, 2026 · Last updated Jul 08, 2026 · Updated 2 times
Summary
This observational study in Germany looks at whether hydrotalcite (Talcid) can ease acid-related symptoms like heartburn that occur when people stop long-term use of proton pump inhibitors (PPIs). About 167 adults who recently stopped PPIs will take hydrotalcite as needed for four weeks and report their symptom relief and satisfaction. The goal is to see if this antacid helps people avoid restarting PPIs.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Hydrotalcite (Talcid chewable tablet)
- What this could lead to
- If successful, this could show that hydrotalcite is an effective on-demand option for managing acid rebound symptoms after stopping PPIs, helping people avoid restarting long-term acid suppression.
- What could go wrong
- This is a small observational study (167 participants) with no control group, so results may not prove cause and effect. The 40% dropout rate could also limit the reliability of findings.
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.
- Participants
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About 167 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2025
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult subjects aged 18 years and older for whom there is not/no longer an indication for a daily PPI therapy according to approval status and guidelines, and who suffer from acid related symptoms due to an acid rebound after discontinuation of a non/no longer indicated long-term PPI-therapy (≥8 weeks).
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Eligibility Criteria: Adult female or male subjects aged ≥ 18 * Subjects who have discontinued daily PPI therapy (≥ 8 weeks of therapy) for which there is no current indication according to guidelines and approval status, e.g. * irritable bowel syndrome * subjects who receive Non-Steroidal Anti-Inflammatory drug (NSAID) treatment with no warning signals\* regarding ulcers * polymedication\*\* with no warning signals\* or side effects regarding ulcers * unclarified upper abdominal discomfort * mild forms of GERD; like Non-Erosive Reflux Disease (NERD), Los Angeles (LA) grade A/B esophagitis * Suffer from acid-rebound due to a discontinuation of a non/no longer indicated long-term PPI therapy (≥ 8 weeks of therapy) * No endoscopically diagnosed GERD\*\*\* * No indication for a PPI-therapy according to guidelines. Examples for guideline recommendations for a PPI-therapy: * moderate - severe forms of reflux esophagitis * gastric ulcer, duodenal ulcer * Helicobacter pylori eradication * moderate/severe forms of GERD - Los Angeles (LA) grade C/D esophagitis * Zollinger-Ellison-Syndrome No Talcid® contraindications or warnings as: * pregnancy and lactation * severe renal impairment * hypophosphatemia * existing myasthenia gravis * impaired renal function * Alzheimer's disease or other forms of dementia * patients under low-phosphate diet * hypersensitivity to the ingredients of Talcid® * Subjects who voluntarily agree to use Talcid® Chewable Tablets for relief of acid-related symptoms due to acid-rebound * Decision to initiate on-demand treatment of acid-related symptoms due to acid-rebound with Talcid® was made as per investigator's routine recommendation practice and by the subject * Subject purchases Talcid® for her/his own use * Signed informed consent * No participation in an investigational program with interventions outside of routine clinical practice * No contraindications according to the local marketing authorization \* Warning signals: * Age \> 60 (with one additional warning signal) * Previous history or family history of ulcers * Helicobacter pylori positive status \*\* Polymedication: defined as at least five medicinal products at the same time for a continuous therapy \*\*\* Endoscopy: LA grade C/ D esophagitis, Barrett esophagus, peptic stricture; pH- Impedance measurement: acid exposure \> 6% Exclusion Criteria: not applicable
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Bayer Germany
NOT_YET_RECRUITINGWuppertal, 42096, Germany
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Bayer Vital GmbH
RECRUITINGLeverkusen, 51373, Germany
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