Viewing Study NCT02668562



Ignite Creation Date: 2024-05-06 @ 8:04 AM
Last Modification Date: 2024-10-26 @ 11:56 AM
Study NCT ID: NCT02668562
Status: COMPLETED
Last Update Posted: 2023-10-26
First Post: 2016-01-06

Brief Title: Timing of Coronary Artery Bypass Surgery Among Patients With Acute Coronary Syndromes Initially on Ticagrelor
Sponsor: Ottawa Heart Institute Research Corporation
Organization: Ottawa Heart Institute Research Corporation

Study Overview

Official Title: Reassessment of Anti-Platelet Therapy Using InDividualized Strategies -Ticagrelor in Patients With Acute Coronary Syndromes Treated by Coronary Artery Bypass Graft Surgery - A Pharmacodynamic and Clinical Study to Decrease Bleeding Risks and Ischemic Complications - The RAPID-TITRATE CABG Study
Status: COMPLETED
Status Verified Date: 2023-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: RAPID CABG
Brief Summary: Ticagrelor a more potent P2Y12 inhibitor has been shown to reduce major adverse cardiac events MACE in acute coronary syndromes ACS It is increasingly used as a first line therapy in ACS However more potent P2Y12 inhibition has been associated with increased bleeding This may be of particular concern for patients with ACS who require coronary artery bypass surgery CABG In particular the timing for cessation of ticagrelor before proceeding to CABG is unclear RAPID TITRATE CABG is a randomized vanguard study to evaluate the feasibility and preliminary safety of a strategy of early versus delayed CABG in ACS patients initially treated with ticagrelor and to identify potential mechanisms underlying benefits or complications of early bypass surgery
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None