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Clinical Trial 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.


Clinical Trial Description

This study is a multicenter, prospective, open-label, blinded endpoint, randomized controlled trial designed to evaluate the effect of immediate angioplasty (with or without stenting) for AIS with severe ICAS. The primary outcome is the proportion of patients with a 90-day modified Rankin scale (mRS) of 0-2. Study intervention: (1) Participants in the experimental group will undergo immediate angioplasty (with or without stenting), and will receive the best medical treatment (BMM) after the procedure. (2) Participants in the control group will receive BMM alone. This study is anticipated to enroll 418 participants, with 209 participants in each group (1:1 ratio). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06437600
Study type Interventional
Source Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Contact Xinguang Yang, MD
Phone 86-20-81332619
Email yangxinguang0926@163.com
Status Not yet recruiting
Phase N/A
Start date October 2024
Completion date December 2029