Multicentre, randomised, double-blind, parallel controlled trial to investigate timing of platelet inhibition after coronary artery bypass grafting: TOP-CABG trial study

Author:

Yuan Xin,Chu QingORCID,Chen Kai,Wang YangORCID,Zhang Lihua,Zheng Yingli,Hu Shengshou

Abstract

IntroductionDual antiplatelet therapy (DAPT), referred to as the combination of aspirin and P2Y12receptor antagonist (clopidogrel or ticagrelor), potentially improves patency of saphenous vein grafts (SVG) after coronary artery bypass grafting (CABG), while it is further proposed that DAPT potentially increases bleeding risk. Compared with DAPT, de-escalated DAPT (De-DAPT) is an effective antiplatelet strategy for acute coronary syndrome treatment, which significantly reduces the risk of bleeding without increasing the incidence of major adverse cardiovascular events. However, insufficient evidence is available to determine the timing of DAPT after CABG.Methods and analysisEthics and disseminationThe Ethics Committee in Fuwai hospital approved this study (2022-1774). Fifteen centres agreed to participate the TOP-CABG trial, and the study has been approved in these 15 centres by whose ethics committee. The results of the trial will be submitted for publication in a peer-reviewed journal.Trial registration numberNCT05380063.

Funder

National Clinical Research Centre of Cardiovascular Diseases

Publisher

BMJ

Subject

General Medicine

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