Skip to main content
. 2001 May 31;2(3):129–140. doi: 10.1186/cvm-2-3-129

Table 2.

Intravenous glycoprotein IIb/IIIa receptor blockers for patients undergoing percutaneous coronary intervention

Primary end point

Trial Patient category n IIb/IIIa Placebo P value
EPIC [72] AMI, UA or high-risk lesion 2099 8.3 12.8 0.008
EPILOG [74] SA 2792 5.2 11.7 < 0.001
CAPTURE [62] Refractory UA 1265 11.3 15.9 0.01
IMPACT-II [77] AMI, SA,UA 4010 9.2 11.4 0.06
RESTORE [78] UA 2139 10.3 12.2 0.16
EPISTENT [103] AMI, UA, SA and stent eligible 2399 5.3 10.8 < 0.001

See text for details of patient selection, primary end points, and outcome. In the EPIC, EPILOG, CAPTURE and EPISTENT trials, the primary end point consisted of death, acute myocardial infarction (AMI) or target vessel revascularization (TVR) at 30 days. In the IMPACT-II trial, the need for a bailout stent also included a primary end point. In the RESTORE trial, not only TVR was included, but any revascularizations. UA, Unstable angina; SA, stable angina.