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Clinical Trial Summary

The aim is to assess the effects and harms of Xueshuantong lyophilized powder versus placebo in patients with acute ischemic stroke when initiated within 72 hours of symptom onset.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04415164
Study type Interventional
Source Dongzhimen Hospital, Beijing
Contact Ying Gao
Phone 0086-010-84013209
Email gaoying973@126.com
Status Recruiting
Phase Phase 4
Start date September 29, 2020
Completion date May 31, 2023

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