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Optimal PERioperative Antiplatelet Therapy Investigation ON Abdominal Surgery After Coronary Stent Implantation
RECRUITINGPhase 4Sponsored by Kyoto University
Actively Recruiting
PhasePhase 4
SponsorKyoto University
Started2025-01-20
Est. completion2027-02-28
Eligibility
Age20 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06723145
Summary
The purpose of this study is to evaluate the impact of perioperative aspirin continuation on clinical outcomes in patients with a history of coronary stent implantation who are scheduled for abdominal surgery.
Eligibility
Age: 20 Years+Healthy volunteers accepted
Inclusion Criteria: * Patients with a history of coronary stenting and scheduled for abdominal surgery * Patients on a single antiplatelet agent Exclusion Criteria: * Patients on dual antiplatelet therapy (DAPT) * Patients on anticoagulation therapy * Patients with a history of stent thrombosis * Patients with CHADS2 score \>= 5 * Patients at extremely high risk of bleeding and unable to continue preoperative aspirin * Patients incapable of consent, including those under 20 years of age * Other patients for whom either discontinuation or continuation of antiplatelet agents is deemed inappropriate by the attending physician
Conditions3
Antiplatelet AgentsHeart DiseasePerioperative Care
Interventions2
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Actively Recruiting
PhasePhase 4
SponsorKyoto University
Started2025-01-20
Est. completion2027-02-28
Eligibility
Age20 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06723145