drugset / Trial / NCT06134622

Advancing Stroke Safety and Efficacy Through Early Tirofiban Administration After Intravenous Thrombolysis (ASSET-IT)

NCT06134622 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

To assess the efficacy and safety of tirofiban administration after intravenous thrombolysis for patients with AIS.

Timeline

Start
2024-03-14
Primary completion
2024-09-25
Completion
2024-12-30

Outcome

Met primary endpoint

paper higher percentage of patients in the tirofiban group than in the placebo group (65.9% vs. 54.9%; risk ratio, 1.20; 95% confidence interval, 1.07 to 1.34; P = 0.001). PMID 40616232 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Tirofiban Other / unclassified 0.1 ug/kg Intravenous

Indications