completed

STRIVE evaluated the use of adjunctive, low-dose intracoronary tissue plasminogen activator during primary percutaneous coronary intervention (PCI) for patients with ST elevation myocardial infarction (STEMI) in reducing major adverse cardiovascular events.

STRIVE assessed the efficacy of a novel approach to prevent and treat microvascular obstruction and reduce major cardiovascular events using intracoronary administration of very low-dose fibrinolytic (tissue plasminogen activator, tPA) directly into the culprit coronary artery during primary PCI.

The objective was to determine if tPA (10 mg or 20 mg combined dose) can reduce the incidence of the composite of post-procedural myocardial blush (MBG) grade 0/1, distal embolization, failure to achieve 50% ST-segment resolution at 30 minutes post-PCI or major adverse cardiovascular events at 30 days in patients undergoing primary PCI for STEMI.

STRIVE Slides - Download PDF
Study Type

Interventional - Drug

Study Design

Prospective, multi-centre, double-blind, RCT

NO. of Countries

1

NO. of Sites

3

NO. of Participants

210

Study Period

2018-2025

Sponsor

PHRI

Heart & Stroke Foundation

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