Clinical Trial

The 10-Year Extended Follow-up of the DACAB Trial

Study acronym: DACAB-FE-10Y
Completed
View on ClinicalTrials.gov →
Summary
The goal of this observational study is to learn about the very long-term effects of different antiplatelet strategies in patients who underwent coronary artery bypass grafting (CABG) and participated in the original DACAB trial. The main questions it aims to answer are: Does one year of treatment with ticagrelor plus aspirin (dual antiplatelet therapy) after CABG reduce the risk of major adverse cardiovascular events (MACE) over 10 years compared with aspirin alone or ticagrelor alone? What are the long-term safety outcomes, including major bleeding events, among patients who received different antiplatelet strategies? Researchers will compare the three originally randomized groups (ticagrelor plus aspirin, ticagrelor alone, and aspirin alone) to see if a one-year course of dual antiplatelet therapy provides a sustained clinical benefit over a decade. Participants will: Be contacted by telephone by the central study team for a one-time follow-up interview. Provide information about their current health status, any cardiovascular events (such as heart attack, stroke, or repeat revascularization procedures) that have occurred since the last follow-up. Report their current use of medications, including antiplatelet and other cardiovascular drugs. Allow researchers to request relevant medical records to verify any reported clinical events.
Protocol Amendment History 3 changes
critical Trial status changed: Enrolling by Invitation → Completed 2026-08-12
notable Primary completion pushed: 2026-04 -> 2026-08 2026-07-10
minor Completion pushed: 2026-06 -> 2026-08 2026-07-10
Trial Details
NCT Number NCT07480629
Lead Sponsor Ruijin Hospital
Conditions Coronary Artery Disease, CABG, Antiplatelet Therapy of Coronary Artery Bypass
Enrollment 500 participants
Start Date 2026-03-15
Primary Completion 2026-07-20 (estimated)
Study Completion 2026-07-30 (estimated)
Updated on ClinicalTrials.gov 2026-08-11