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ProUrokinase in Mild IsChemic strokE (PUMICE) — PUMICE  

Ischemic Stroke Clinical Trial

Official title:
Recombinant Human Prourokinase（rhPro-UK）for Injection Versus Standard Medical Treatment for Acute Mild Ischemic Stroke (NIHSS≤5) Within 4.5 Hours After Symptom Onset

Clinical Trial Summary

The purpose of this study is to investigate the safety and efficacy of rhPro-UK (35mg) versus standard medical treatment in acute mild ischemic stroke within 4.5 hours of symptom onset.

Clinical Trial Description

After being informed about the study and potential risks, patients who meet the eligibility requirements will be randomized to recombinant human Prourokinase for injection (rhPro-UK) or standard medical treatment in a 1:1 ratio. Written informed consent will be needed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05507645
Study type Interventional
Source Beijing Tiantan Hospital
Contact yongjun wang, MD
Phone 13911172565
Email yongjunwang111@aliyun.com
Status Recruiting
Phase Phase 3
Start date October 21, 2022
Completion date June 2024
View Details
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