Optimal PERioperative Antiplatelet Therapy Investigation ON Abdominal Surgery After Coronary Stent Implantation

Recruiting Phase 4 Interventional Study
Antiplatelet Agents Perioperative Care
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
20 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
1,200 (estimated)
Sponsor
Kyoto University · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

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.

Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
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 *…
Contacts

Hiroki Shiomi, MD, PhD

+81-75-751-4255

hishiomi@kuhp.kyoto-u.ac.jp

CONTACT

Erika Yamamoto, MD, PhD

+81-75-751-4254

erkymmt@kuhp.kyoto-u.ac.jp

CONTACT