| Literature DB >> 29897428 |
Hector M Garcia-Garcia1,2, Eugène P McFadden3, Andrew Farb4, Roxana Mehran5, Gregg W Stone6, John Spertus7, Yoshinobu Onuma1, Marie-Angèle Morel1, Gerrit-Anne van Es1, Bram Zuckerman4, William F Fearon8, David Taggart9, Arie-Pieter Kappetein10, Mitchell W Krucoff11, Pascal Vranckx12, Stephan Windecker13, Donald Cutlip14, Patrick W Serruys15.
Abstract
The Academic Research Consortium (ARC)-2 initiative revisited the clinical and angiographic end point definitions in coronary device trials, proposed in 2007, to make them more suitable for use in clinical trials that include increasingly complex lesion and patient populations and incorporate novel devices such as bioresorbable vascular scaffolds. In addition, recommendations for the incorporation of patient-related outcomes in clinical trials are proposed. Academic Research Consortium-2 is a collaborative effort between academic research organizations in the United States and Europe, device manufacturers, and European, US, and Asian regulatory bodies. Several in-person meetings were held to discuss the changes that have occurred in the device landscape and in clinical trials and regulatory pathways in the last decade. The consensus-based end point definitions in this document are endorsed by the stakeholders of this document and strongly advocated for clinical trial purposes. This Academic Research Consortium-2 document provides further standardization of end point definitions for coronary device trials, incorporating advances in technology and knowledge. Their use will aid interpretation of trial outcomes and comparison among studies, thus facilitating the evaluation of the safety and effectiveness of these devices.Entities:
Mesh:
Year: 2018 PMID: 29897428 DOI: 10.1093/eurheartj/ehy223
Source DB: PubMed Journal: Eur Heart J ISSN: 0195-668X Impact factor: 29.983