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 18 or older (there is no upper age limit)
- People showing signs consistent with an acute ischemic stroke (a stroke caused by a blood clot blocking blood flow to the brain)
- People with a stroke severity score above 5 at the time of enrolment, where the last time they were known to be well was within the past 23 hours — or people with symptoms that have been coming and going, or gradually getting worse, over the last 7 days
- People whose ischemic stroke has been confirmed by a brain scan (CT or MRI), or whose scan appears normal but a stroke is still suspected
- People whose brain scan shows a specific pattern suggesting a portion of the brain is at risk but not yet fully damaged, meeting certain size and ratio thresholds (confirm with trial site for exact technical details)
- People whose imaging (CT or MRI angiography) shows a complete blockage of the internal carotid artery in the neck, from any cause (such as a tear in the artery wall, plaque build-up, or unknown cause), without a related blockage of a large artery inside the skull, confirmed within 1 hour before enrolment
- People for whom the procedure to treat the blockage is expected to be able to start within 60 minutes of enrolment
- People who were able to live independently or with only minor limitations before the stroke (pre-stroke disability score of 2 or less out of 5)
- People, or their legal representative, who have been informed about the study and have given signed consent, or who meet the criteria for emergency consent
Who may not be able to join:
- People who had a surgical procedure to clear their carotid artery (endarterectomy) within the past month
- People with serious or life-threatening other health conditions, or a life expectancy of less than 6 months, where the procedure is unlikely to be of benefit
- People who would be unable to attend follow-up appointments
- People with a pre-existing neurological or psychiatric condition that would make it difficult to accurately assess stroke-related symptoms
- People who had a seizure at the start of the stroke, if it makes the stroke diagnosis uncertain or prevents an accurate baseline assessment
- People where a disease affecting the blood vessels of the brain (such as inflammation of the blood vessels) is suspected based on medical history or imaging
- People who are currently pregnant, planning to become pregnant during the study period, or who are breastfeeding at the time of admission
- People who are legally protected adults or under guardianship (confirm with trial site)
- People currently taking part in another clinical trial of an investigational medicine or device
- People who are not affiliated with or covered by the French social security system
- People with a known life-threatening allergy to contrast dye or endovascular products used in the procedure
- People who also have a narrowing of 50% or more in the middle cerebral artery on the same side as the carotid blockage
- People whose carotid artery was already known to be blocked 30 or more days before enrolment, or where the blockage is strongly suspected to be long-standing based on history or imaging
- People who have both a neck carotid artery blockage and a large artery blockage inside the skull at the same time
- People with a previous stent already placed in the affected carotid artery
- People with a stent already in a brain artery in the same area as the carotid blockage
- People where the carotid artery is severely narrowed but not fully blocked (sub-occlusive stenosis) on imaging
- People where the blockage is suspected to start in a deeper portion of the carotid artery (inside the skull or at the base), while the neck portion appears normal on imaging
- People with no usable vascular access point for the procedure
- People where an aortic dissection (a tear in the main artery from the heart) is suspected based on history, examination, or imaging
- People where the common carotid artery (a different artery in the neck) is blocked but the internal carotid artery is not
- People whose brain scan shows any sign of bleeding in the brain
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: 0033467330204
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
Percentage of patients with favorable functional outcome, defined by a mRS score ≤2
Can't join this trial?
Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.