Heart monitor could make blood thinners safer for heart attack patients

NCT ID NCT04276155

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether an implantable heart monitor with remote follow-up can help doctors decide when to prescribe blood thinners to patients who have had a heart attack and developed new atrial fibrillation. The goal is to reduce bleeding complications compared to the standard approach of giving blood thinners based on a risk score. About 500 participants will be randomly assigned to either standard care or the implantable monitor strategy.

What this could mean

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

Active substance
implantable heart monitor with remote follow-up
What this could lead to
If successful, this could lead to a safer way to decide when to use blood thinners in heart attack patients with atrial fibrillation, reducing bleeding risks.
What could go wrong
This is a Phase 4 study, so the approach is already in use, but it may not prove safer than standard care. The implant device itself carries small risks like infection or malfunction.

This is an AI summary of the original study and may miss details. Read our disclaimer.

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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

  • Centre Hospitalier d'Aix en Provence

    Aix-en-Provence, France

  • Centre Hospitalier d'Annecy Genevois

    Metz-Tessy, France

  • Centre Hospitalier d'Haguenau

    Haguenau, France

  • Centre Hospitalier de La Rochelle

    La Rochelle, France

  • Centre Hospitalier de Libournes

    Libourne, France

  • Centre Hospitalier de Périgueux

    Périgueux, France

  • Centre hospitalier Chartres Louis Pasteur le Coudray

    Chartres, France

  • Centre hospitalier de Pau

    Pau, 64046, France