Clinical Trial

Urokinase for Thrombolysis in Acute Ischemic Stroke

Recruiting
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Summary
According to the Chinese Guidelines for the Diagnosis and Treatment of Ischemic Stroke, intravenous thrombolysis with urokinase, administered at doses of 1-1.5 million IU within 6 hours of symptom onset, has been shown to be both safe and effective for patients with acute ischemic stroke. Compared to alteplase, urokinase offers considerable cost advantages while maintaining comparable therapeutic efficacy. However, current dosing protocols in clinical practice largely rely on the empirical judgment of physicians rather than evidence-based standardization. Therefore, the development of a weight-adjusted dosing regimen for urokinase is of significant clinical importance in optimizing treatment outcomes and ensuring patient safety. The purpose of this study is to determine the maximum tolerated dose of urokinase thrombolytic treatment in patients with acute ischemic stroke and to develop an optimal weight-adjusted dosing regimen.
Protocol Amendment History 4 amendments
This ClinicalTrials.gov record has been amended 4 times since 2025-06-24; most recent amendment 2026-07-13.
Status change: Not Yet Recruiting → Recruiting 2025-09-24
Trial Details
NCT Number NCT07047326
Lead Sponsor Capital Medical University
Conditions Acute Ischemic Stroke
Enrollment 24 participants
Start Date 2025-10-01
Primary Completion 2026-10-02 (estimated)
Study Completion 2027-01-02 (estimated)
Updated on ClinicalTrials.gov 2026-07-14