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 18 or older
- People experiencing symptoms of an acute ischemic stroke (a stroke caused by a blocked blood vessel)
- People whose imaging (CTA or MRA scan) has confirmed a blockage in a specific artery supplying the front part of the brain (the intracranial carotid artery or certain segments of the middle cerebral artery)
- People who are enrolled in the trial within 24 hours of when their stroke symptoms started, or within 24 hours of when they were last known to be well
- People who were able to live mostly independently before the stroke (a pre-stroke disability score of 2 or less on a standard scale)
- People with a stroke severity score of 6 or higher at the time of enrolment, indicating at least a moderate stroke
- People whose brain scan shows that a sufficient amount of brain tissue is still potentially salvageable (an ASPECTS score of 3 or higher)
- People who have provided signed informed consent to participate
Who may not be able to join:
- Women who are pregnant or breastfeeding
- People with a known allergy to contrast dye used in medical scans, or to nitinol (a metal used in some medical devices)
- People with a known allergy to midazolam or related medicines (benzodiazepines)
- People with a known allergy to dexmedetomidine or any of its ingredients
- People who are planned to receive full general anaesthesia for their stroke procedure
- People with blood pressure that is too high or too low and cannot be controlled (systolic above 185 or below 90 mmHg, or diastolic above 110 or below 60 mmHg)
- People with certain heart rhythm problems, specifically second- or third-degree heart block, or a resting heart rate below 50 beats per minute
- People who have had major surgery or a serious injury within the past 14 days
- People with a known bleeding disorder, or blood test results showing low platelet count or abnormal clotting measures
- People with blood sugar levels that are dangerously low or very high
- People with severe kidney disease or very poor kidney function
- People currently receiving kidney dialysis (haemodialysis or peritoneal dialysis)
- People whose life expectancy is less than one year
- People experiencing severe agitation or seizures at the time of enrolment
- People showing signs of inflammation of the blood vessels in the brain (central nervous system vasculitis)
- People with a pre-existing neurological condition or mental health disorder that would make it difficult to assess the effects of the treatment
- People who are unwilling to attend a follow-up assessment at 90 days
- People already participating in another interventional clinical trial
- People whose brain scan shows any bleeding in the brain
- People whose scan shows a cerebellar stroke (stroke in the back of the brain) that is causing significant swelling or pressure
- People with an untreated or incompletely treated brain aneurysm or abnormal blood vessel formation in the brain
- People with blockages in multiple brain blood vessels, or blockages on both sides of the brain
- People with a brain tumour that is causing pressure or swelling 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
Principal Investigator: Xinfeng Liu, Department of Neurology, Jinling Hospital, China
Phone: +86 2584801861
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 mRS score 0-2 at 90 days
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.