Phase 4 Stroke Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People aged 65 or older who have had a stroke caused by a blockage in the brain within the last 15 days, confirmed by an MRI or CT scan
- People who have not been previously diagnosed with atrial fibrillation (an irregular heartbeat), and where no atrial fibrillation was detected during their hospital stay
- People where atrial fibrillation is suspected based on one or more of the following: multiple strokes across different areas of the brain; a single stroke plus blockages found in other organs like the kidneys, spleen, or limbs; certain heart measurements or test results suggesting irregular heart activity (confirm with trial site for specific values); or people aged 80 or older who have had a single stroke
- People who have a plan in place to monitor their heart rhythm over a long period, such as a wearable heart monitor or an implanted recording device
- People whose level of disability after stroke is rated 4 or below on a standard scale (meaning they may need some help with daily activities but are not completely dependent)
- People who have given their written agreement to take part in the trial
- People who are enrolled in the French social security system
Who may not be able to join:
- People whose stroke already has a clearly identified cause, based on a specific medical classification system used by doctors (confirm with trial site)
- People who have had a brain bleed that caused symptoms (the presence of very small, silent bleeds on a specialised scan alone does not automatically exclude someone)
- People with high blood pressure that is not under control, as judged by the treating doctor
- People for whom there is already a clear medical reason to take blood-thinning or anti-clotting medication
- People for whom blood-thinning or anti-clotting medication is medically not suitable
- People with another serious illness that might affect the trial results or prevent them from attending follow-up visits
- People already taking part in another clinical trial involving a treatment intervention
- People of childbearing potential who are not using contraception
- People who are under legal guardianship or a court-appointed support arrangement
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 1 40 25 87 25
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Occurrence of fatal or nonfatal ischemic stroke, or peripheral emboli (even if asymptomatic) [peripheral emboli: emboli in arm or leg, new renal, splenic, hepatic, mesenteric infarction]
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.