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Xingnaojing for Mild-to-severe Acute Ischemic Stroke — XMAS-2  

Acute Ischemic Stroke Clinical Trial

Official title:
Xingnaojing for Mild-to-severe Acute Ischemic Stroke (XMAS-2): A Multicenter, Randomized, Double-blind, Placebo-Controlled Trial

Clinical Trial Summary

The main purpose of this trial is to determine whether Xingnaojing, intravenously administered within 24 hours of symptom onset, improves the daily living ability of acute ischemic stroke at 90 days.

Clinical Trial Description

The XMAS-2 study is a multicenter, randomized, double-blind, placebo-controlled clinical trial. The primary hypothesis of this trial is that Xingnaojing will improve the daily living ability of acute ischemic stroke at 90 days. Xingnaojing will be compared to placebo, combined with guidelines-based standard care in patients with acute ischemic stroke within 24 hours of symptom onset. All participants will have a National Institutes of Health Stroke Scale(NIHSS)entry score of 4-25. Participants who have planned or already received the intravenous thrombolysis or endovascular treatment will be excluded. The primary outcome will be determined at 90 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04150835
Study type Interventional
Source Dongzhimen Hospital, Beijing
Contact Ying Gao, MD
Phone 0086-010-84013209
Email gaoying973@126.com
Status Recruiting
Phase Phase 4
Start date March 19, 2020
Completion date December 2021
View Details
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