Phase 3 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
- People who have a confirmed blockage in a major blood vessel supplying the front part of the brain (specifically the internal carotid artery or a main branch of the middle cerebral artery), confirmed by a specialised type of scan (CTA or MRA)
- People for whom a procedure to remove the blood clot is considered appropriate within 12 hours of symptoms starting
- People whose stroke is strongly suspected to be caused by a build-up of fatty deposits (plaque) in the arteries, based on their medical history, symptoms, and scan results
- People with a stroke severity score of 6 or higher on a standard medical scale (NIHSS) at the start
- People whose brain scan shows a score of 6 or higher on a measure of how much brain tissue is still healthy (ASPECTS)
- People who were largely independent in daily life before the stroke (a functional score of 2 or less on a standard scale called the mRS)
- People (or their legal representative) who have signed a consent form agreeing to take part
Who may not be able to join:
- People who have a history of irregular heart rhythms called atrial fibrillation or atrial flutter, or whose heart tracing (ECG) shows these rhythms after admission
- People who have had a bleeding-type stroke (such as a brain bleed or bleeding around the brain), or any bleeding event in the past month
- People who have brain aneurysms, abnormal blood vessel formations in the brain, very twisted arteries that would make the clot-removal procedure difficult, or brain tumours that are causing pressure in the skull
- People who have taken certain blood-thinning or antiplatelet medications in the past week, including dual antiplatelet therapy, direct oral anticoagulants, or warfarin
- People with severely uncontrolled high blood pressure (top number above 200 mmHg or bottom number above 110 mmHg)
- People with certain blood clotting problems, a key clotting measurement (INR) above 1.7, or a low platelet count (below 90×10⁹/L)
- People with severe kidney problems or a serious illness where life expectancy is less than 6 months
- People who are pregnant or breastfeeding
- People with known allergies to medications or contrast dyes used in scans
- People already taking part in another clinical trial
- People whom the research team considers unsuitable for other reasons (confirm with trial site)
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: +86-024-28897511
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
The proportion of patients with functional independence (modified Rankin Scale [mRS] score of 0 to 2)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 9 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.