Efficacy and Safety of Short Duration of DAPT After GENOSS® DES Implantation in Patients with Coronary Artery Disease
NCT06075420 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000
Last updated 2025-02-21
Summary
The objective of study is to evaluate the efficacy and safety of short duration of DAPT after GENOSS® DES Implantation in patients with coronary artery disease.
Conditions
- Percutaneous Coronary Intervention
- Dual Antiplatelet Therapy
Sponsors & Collaborators
-
Genoss Co., Ltd.
lead INDUSTRY
Eligibility
- Min Age
- 19 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-08-18
- Primary Completion
- 2027-12-31
- Completion
- 2027-12-31
Countries
- South Korea
Study Locations
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