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New study tests antacid for Post-PPI acid rebound relief

NCT ID NCT07291700

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

About 167 people

The number the study aims to enrol. It can still change while the study runs.

Started

Nov 2025

Expected to finish

Oct 2026

An estimate. End dates often move.

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

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.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Bayer Germany

    NOT_YET_RECRUITING

    Wuppertal, 42096, Germany

  • Bayer Vital GmbH

    RECRUITING

    Leverkusen, 51373, Germany

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