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.