Clinical Trials Directory

Trials / Recruiting

RecruitingNCT03789916

SAPT Versus DAPT in Incomplete Revascularization After CABG

Single Versus Dual Antiplatelet Therapy in Patients With Incomplete Revascularization After Coronary Artery Bypass Graft Surgery

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
800 (estimated)
Sponsor
Campus Bio-Medico University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study aims to compare the efficacy of dual antiplatelet therapy (DAPT) over single antiplatelet therapy (SAPT) in patients with incomplete revascularization after coronary artery bypass graft surgery (CABG). Before hospital discharge, patients will be 1:1 randomized to SAPT (acetylsalicylic acid 100 mg/die) or DAPT (acetylsalicylic acid 100 mg/die + ticagrelor 90 mg bis in die). DAPT will be continued for 12 months, and ticagrelor will be withdrawn thereafter. Primary endpoint is the evaluation of cardiac-related mortality at 5 years from hospital discharge.

Conditions

Interventions

TypeNameDescription
DRUGTicagrelor90 mg bis in die
DRUGacetylsalicylic acid100 mg die

Timeline

Start date
2019-01-02
Primary completion
2021-08-01
Completion
2026-12-31
First posted
2018-12-31
Last updated
2022-07-21

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT03789916. Inclusion in this directory is not an endorsement.

SAPT Versus DAPT in Incomplete Revascularization After CABG (NCT03789916) · Clinical Trials Directory