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EGACY

Phase 1
Recruiting
Conditions
on-ST-segment elevation acute coronary syndrome
Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14]
Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Therapeutics [E02]
Registration Number
CTIS2023-504360-42-00
Lead Sponsor
Amsterdam UMC
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
3090
Inclusion Criteria

Clinical diagnosis of NSTE-ACS (i.e. NSTEMI or unstable angina), Successful PCI (according to the treating physician)

Exclusion Criteria

Known allergy or contraindication for aspirin or all commercially available P2Y12-inhibitors (i.e. ticagrelor, prasugrel and clopidogrel), Concurrent use of oral anticoagulants (e.g. because of atrial fibrillation), Ongoing indication for DAPT at admission (e.g. due to recent PCI or ACS), Planned surgical intervention within 12 months of PCI, Pregnant or breastfeeding women at time of enrolment, Participation in another trial with an investigational drug or device

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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