Clinical Trials Directory

Trials / Completed

CompletedNCT02668562

Timing of Coronary Artery Bypass Surgery Among Patients With Acute Coronary Syndromes Initially on Ticagrelor

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
Phase
N/A
Study type
Interventional
Enrollment
143 (actual)
Sponsor
Ottawa Heart Institute Research Corporation · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
PROCEDUREEarly CABG (Day 2-3 after ticagrelor discontinuation)Timing for CABG after ticagrelor discontinuation
PROCEDUREDelayed CABG (Day 5-7 after ticagrelor discontinuation)Timing for CABG after ticagrelor discontinuation

Timeline

Start date
2016-02-01
Primary completion
2021-04-09
Completion
2022-03-09
First posted
2016-01-29
Last updated
2023-10-26

Locations

2 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT02668562. Inclusion in this directory is not an endorsement.