drugset / Trial / NCT01498003

Tirofiban in Stenting for Long Coronary Lesion

NCT01498003 ↗

Phase 4 Completed 748 enrolled Shanghai Jiao Tong University School of Medicine
RandomizedParallel-groupOpen-labelTreatment

Summary

Periprocedural myonecrosis or infarction are associated with short, intermediate, and long term adverse outcomes. Previous study indicated 12.6% of patients suffered a peri-procedural CK-MB rise by overlapping use of drug-eluting stents for long coronary lesions. Here the investigators hypothesize that peri-procedural use of tirofiban could reduce the occurrence of periprocedural infarciton in elective patients with long coronary lesions treated by overlapping use of drug-eluting stents.

Timeline

Start
2011-11
Primary completion
2014-06
Completion
2014-06

Outcome

Met primary endpoint

paper the primary endpoint was significantly reduced in the tirofiban group (4.0% vs. 11.5%, P < 0.001). PMID 25630513 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Tirofiban Other / unclassified 0.15 ug/kg Intravenous