Can an implanted heart monitor catch hidden irregular heartbeats after stroke?
NCT ID NCT05717504
First seen Sep 18, 2026 ยท Last updated Sep 18, 2026
Summary
Researchers are testing whether an implanted loop recorder can detect atrial fibrillation in people who have had a stroke. The device continuously monitors heart rhythm for up to a year or longer. The pilot trial enrolls 24 patients across three centers to see if a larger study of more than 1,000 people is feasible. Participants also complete a quality-of-life survey.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- an implantable loop recorder, a small device placed under the skin to continuously monitor heart rhythm
- What this could lead to
- If the approach works, it could help doctors detect irregular heartbeats after a stroke and guide treatment to prevent another stroke.
- What could go wrong
- This is a small pilot trial with 24 patients, so it cannot prove that long-term monitoring improves outcomes. Implanting a device carries small risks of infection or discomfort, and the study may show that a larger trial is not practical.
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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.
- Expected to start
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Nov 2023
An estimate. Start dates often move.
- Expected to finish
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Feb 2025
An estimate. End dates often move.
- 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.
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.
Inclusion Criteria: \- Adult patients with cortical or subcortical, cryptogenic or non-cryptogenic acute ischemic stroke Exclusion Criteria: * AF on 24-h inpatient or Holter monitoring * Atrial or ventricular thrombus * Other major-risk cardioembolic sources (e.g., mechanical valve) * Other indications (e.g., venous thromboembolism) or contraindications for OACs.
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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.
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Other studies related to the condition(s) this trial covers.
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