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Gut bacteria fix may boost heart drug power

NCT ID NCT07203846

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a short course of the antibiotic rifaximin can improve how well the blood thinner ticagrelor works in people who have had a heart attack. The idea is that unhealthy gut bacteria may interfere with the drug, and clearing them out could help prevent future clots. The trial will enroll 50 adults who are already taking ticagrelor and have high platelet reactivity, meaning their blood is still too sticky.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
rifaximin (an antibiotic)
What this could lead to
If it works, this could point toward a way to make standard blood thinners work better for heart attack survivors by adjusting gut bacteria.
What could go wrong
This is a small, early-phase trial with only 50 people. The antibiotic may not improve blood thinning, or could cause side effects like stomach upset or antibiotic resistance.

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

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

About 50 people

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

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Jun 2027

An estimate. End dates often move.

Lead sponsor

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

18 to 80 years

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.

Inclusion criteria: * Between 18 and 80 years of age * History of acute coronary syndrome no sooner than 1 month and no later than 12 months prior to study inclusion * Current treatment with ticagrelor (90 mg orally twice a day) * High platelet reactivity assessed with multiple electrode aggregometry method (AUC of \>46 U) * Provision of informed consent prior to any study procedures Exclusion criteria: * History of hypersensitivity to rifaximin or other rifamycin-derived agent * Ongoing treatment with rifamycins * Platelet count \< 100×10\^9/L or \> 450×10\^9/L * Treatment with antibiotics, probiotics, or glucocorticoids within 3 months prior to study inclusion * History of gastrointestinal diseases such as inflammatory bowel disease, bowel obstruction, or gastrointestinal tumor * Infection, including gastrointestinal infection, within a month prior to study inclusion * History of Clostridium difficile infection * Current use of specific medications (warfarin, glycoprotein IIb/IIIa inhibitors, immunosuppressants, bile acid sequestrants, antidiarrheal agents) * Impaired liver function classified as Child-Pugh class B or C * Hemodynamic instability * Pregnancy or breastfeeding * Patients considered by the investigator to be uncooperative

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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

    1 site. 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.

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  3. A doctor treating you

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Contacts and locations

Locations

  • Cardiology Department, Dr. A. Jurasz University Hospital

    Bydgoszcz, Cuiavian-Pomeranian, 85-094, Poland

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