drugset / Trial / NCT04415164

Evaluation of Xueshuantong in Patients With AcutE IschemiC STroke

NCT04415164 ↗

RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2020-09-29
Primary completion
2022-10-31
Completion
2023-05-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Xueshuantong Unknown 500 mg Intravenous

Indications