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Clinical Trials/CTIS2023-508148-23-01
CTIS2023-508148-23-01
Active, not recruiting
Phase 1

Antiplatelet therapy after successful percutaneous coronary intervention for chronically occluded coronary artery: A prospective, multicentre, randomized study comparing two durations of dual antiplatelet therapy - Etude DAPT-CTO

Assistance Publique Hopitaux De Marseille0 sites660 target enrollmentFebruary 7, 2024

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Assistance Publique Hopitaux De Marseille
Enrollment
660
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 7, 2024
End Date
TBD
Last Updated
last year
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients who underwent a successful coronary stent implantation for chronic coronary occlusion, eligible for long\-term aspirin therapy and requiring a dual antiplatelet therapy, Affiliated to Social Security system, Signature of informed consent, Age \> 18 years old

Exclusion Criteria

  • Dual antiplatelet therapy contra\-indication, Patient with hypersensitivity to aspirin (or any of its excipients) and/or to any of the active substance or to any of the excipients of the investigational medical product used in this study (clopidogrel), Patient with contraindication to aspirin and/or clopidogrel, No coronary stent implanted, Age\<18years, Patient under guardianship, Pregnancy or breast feeding, Prasugrel or ticagrelor use

Outcomes

Primary Outcomes

Not specified

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