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Study identifier: NCT03789916 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

SAPT Versus DAPT in Incomplete Revascularization After CABG

Condition: Coronary Artery Disease  ·  Sponsor: Campus Bio-Medico University

PhasePhase 3
Planned participants800
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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 DAPT will be continued for 12 months, and ticagrelor will be withdrawn thereafter.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.

This description comes directly from the study's public registry record.

Talk to the study team

Antonio Nenna, MD  ·  +393337014743  ·  a.nenna@unicampus.it

Massimo Chello, MD  ·  m.chello@unicampus.it

Always discuss trial participation with your own doctor first.

Locations (1)

Università Campus Bio-Medico di RomaRome, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT03789916