The Pivotal Study of the Aptus Endovascular AAA Repair System
NCT00507559
Abdominal Aortic Aneurysms (AAA), Aneurysm
Albany, New York, United States
View Trial DetailsNCT Number: NCT06876727
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.
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All sexes
Observational
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 1 year after EVAR
composite of all-cause death, myocardial infarction (MI), or ischemic stroke
Time frame: 1 year after EVAR
Diagnostic codes in the primary or secondary position and transfusion receipt
Time frame: 1 year after EVAR
Re-intervention or surgery for AAAs
Samsung Medical Center
Other
A Target Trial Emulation for Efficacy and Safety of Antiplatelet Therapy After Endovascular Aortic Repair
Acronym: EVAR_DAPT_SAPT
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