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Efficacy and Safety of Antiplatelet Therapy After Endovascular Aortic Repair

A Target Trial Emulation for Efficacy and Safety of Antiplatelet Therapy After Endovascular Aortic Repair

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06876727
Acronym
EVAR_DAPT_SAPT
Enrollment
8325
Registered
2025-03-14
Start date
2003-01-01
Completion date
2023-09-30
Last updated
2025-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abdominal Aortic Aneurysms (AAA), Endovascular Aneurysm Repair (EVAR)

Keywords

Abdominal Aortic Aneurysms (AAA), Endovascular Aneurysm Repair (EVAR), Single antiplatelet therapy, Dual antiplatelet therapy

Brief summary

This study was a target trial emulation using the National Health Claims database established by the Korean National Health Insurance Service (K-NHIS). 8,325 patients were included.

Detailed description

Among these patients, any patients who were prescribed SAPT or DAPT at the date of discharge from the index hospitalization for standard EVAR were defined as being in the SAPT group (N=4,162) and the DAPT group (N=4,163), respectively.

Interventions

None listed

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients who underwent EVAR for AAA and were successfully discharged

Exclusion criteria

* Patients who had experienced a myocardial infarction * Patients who had experienced a stroke * Patients who had experienced percutaneous coronary intervention * Patients who had history of peripheral disease * Patients who had major bleeding event within 1 year of admission * Those prescribed non-vitamin K antagonist oral anticoagulant or warfarin * Patients who did not prescribe any antiplatelet therapy

Design outcomes

Primary

MeasureTime frameDescription
Major adverse cardiac and cerebrovascular events (MACCE)1 year after EVARcomposite of all-cause death, myocardial infarction (MI), or ischemic stroke
Major or clinically relevant non-major bleeding1 year after EVARDiagnostic codes in the primary or secondary position and transfusion receipt
Re-intervention or surgery for AAAs1 year after EVARRe-intervention or surgery for AAAs

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026