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Bivalirudin With Prolonged Full Dose Infusion Versus Heparin Alone During Emergency PCI — BRIGHT-4  

ST Elevation Myocardial Infarction Clinical Trial

Official title:
Bivalirudin With Prolonged Full Dose Infusion Versus Heparin Alone During: a Multicenter, Randomized, Open-label Trial

Clinical Trial Summary

This study is aimed to investigate if the bivaliruding with prolonged full dose infusion after PCI is superior to heparin alone in reducing 30-day mortality or major bleeding for patients with STEMI treated with emergency PCI. A total of 6000 STEMI patients will be enrolled and randomly assigned to receive bivalirudin or heparin during emergency PCI in a 1:1 ratio. This study will provide key evidence for peri-operative anticoagulant therapy decisions in STEMI patients.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03822975
Study type Interventional
Source Shenyang Northern Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date February 14, 2019
Completion date May 6, 2023
View Details
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