Immediate Angioplasty For Acute Ischemic Stroke With Severe Intracranial Atherosclerotic Stenosis (MAGIC): A Multicenter, Prospective, Open-label, Blinded Endpoint, Randomized Controlled Trial

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

A multicenter, prospective, open-label, blinded endpoint, randomized controlled trial that aims to evaluate the effect of immediate angioplasty (with or without stenting) for acute ischemic stroke (AIS) with severe intracranial atherosclerotic stenosis (ICAS) in improving the 90-day functional outcome.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Aged 18 years or older.

• Diagnosed with AIS and baseline NIHSS ≥6.

• Pre-stroke mRS ≤2.

• Time from symptom onset to randomization ≤ 24 hours; the onset time refers to Last Known Well (LKW).

• Non-contrast CT ASPECTS score ≥6.

• CTA confirmed severe ICAS (70-99%) of the intracranial segment of the internal carotid artery, or M1 or M2 segment of the middle cerebral artery, and is presumed to be responsible for the stroke.

• Informed consent signed by the patient or authorized representative.

Locations
Other Locations
China
Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University
RECRUITING
Guangzhou
Shenzhen Hospital of Southern Medical University
RECRUITING
Shenzhen
Contact Information
Primary
Xinguang Yang, M.D.
yangxinguang0926@163.com
86-20-81332619
Backup
Xiongjun He, M.D., Ph.D.
drxjhe@163.com
Time Frame
Start Date: 2025-05-08
Estimated Completion Date: 2029-12
Participants
Target number of participants: 412
Treatments
Experimental: The intervention group
Participants will receive immediate angioplasty (with or without stenting) for the culprit vessel and the target residual stenosis should be less than 50%. All participants will receive the best medical treatment (BMT).
No_intervention: The control group
Participants will receive BMT alone.
Related Therapeutic Areas
Sponsors
Leads: Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Collaborators: Shenzhen Hospital of Southern Medical University

This content was sourced from clinicaltrials.gov