Viewing Study NCT06437600



Ignite Creation Date: 2024-06-16 @ 11:49 AM
Last Modification Date: 2024-10-26 @ 3:31 PM
Study NCT ID: NCT06437600
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-05-31
First Post: 2024-05-27

Brief Title: Immediate Angioplasty For Acute Ischemic Stroke With Severe Intracranial Atherosclerotic Stenosis
Sponsor: Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Organization: Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Study Overview

Official Title: Immediate Angioplasty For Acute Ischemic Stroke With Severe Intracranial Atherosclerotic Stenosis MAGIC A Multicenter Prospective Open-label Blinded Endpoint Randomized Controlled Trial
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: MAGIC
Brief 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
Detailed 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 11 ratio

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None