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Clinical Trial Summary

This study is aiming to evaluate the efficacy and safety of Huatuo Zaizao pill in ischemic stroke patients who diagnosed as the phlegm and blood-stasis blocking collaterals syndrome in TCM. A total of 80 subjects will be randomly assigned to Huatuo Zaizao pill group or the control group.


Clinical Trial Description

This is a prospective, randomized controlled clinical trial. Eighty patients with phlegm and blood stasis block syndrome of ischemic stroke were randomly assigned to Hua Hua reconstruction group or control group at a ratio of 1:1. The treatment period is 12 weeks. The purpose is to evaluate its efficacy and safety, provide an objective basis for precise treatment of traditional Chinese medicine, and improve clinical efficacy. The main result is the changes of NIHSS, Fugl-Meyer, and MAS 90 days after taking the drug. The secondary result is the change in ADL and TCM symptom scale (CM-SS). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04910256
Study type Interventional
Source Xiyuan Hospital of China Academy of Chinese Medical Sciences
Contact Yanqiu Ding
Phone (+86)18513123006
Email [email protected]
Status Not yet recruiting
Phase Phase 3
Start date June 1, 2021
Completion date July 20, 2022

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