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Clinical Trial Summary

The purpose of this study is to assess the safety and efficacy of early administration of tirofiban in patients treated with tenecteplase for acute ischemic stroke.


Clinical Trial Description

Intravenous thrombolysis with alteplase is recommended in treatment guidelines for patients with acute ischemic stroke. Previous studies showed that intravenous tenecteplase (0.25 mg/kg) is a reasonable alternative to alteplase for all patients presenting with acute ischemic stroke who meet standard criteria for thrombolysis. After thrombolysis-induced recanalisation, reocclusion occurs in 14-34% of patients, probably because of platelet activation. Early administration of antiplatelet therapy after intravenous thrombolysis could reduce the risk of reocclusion and improve outcome. The purpose of this study is to assess the safety and efficacy of early administration of tirofiban in patients treated with tenecteplase for acute ischemic stroke. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05604638
Study type Interventional
Source Second Affiliated Hospital of Guangxi Medical University
Contact Shengliang Shi, MD
Phone +8613707888628
Email ssl_1964@163.com
Status Not yet recruiting
Phase Phase 4
Start date March 31, 2023
Completion date December 31, 2025

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