Trials / Recruiting
RecruitingNCT06577896
The Study to Evaluate the Safety and Efficacy of the Onyx Family
Safety and Efficacy of 1-month Dual Antiplatelet Therapy in High Bleeding and Ischemic Risk Elderly Patients With Coronary Artery Disease After Implantation of Zotarolimus-eluting Coronary Stent System (Onyx Family, Medtronic, Minneapolis, MN); A Multicenter, Prospective, Observational Study
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 500 (estimated)
- Sponsor
- Pusan National University Yangsan Hospital · Academic / Other
- Sex
- All
- Age
- 75 Years – 100 Years
- Healthy volunteers
- Not accepted
Summary
Observation of the safety and efficacy of 1-month dual antiplatelet therapy (DAPT) after percutaneous coronary intervention using Onyx family stents in elderly patients aged 75 years or older
Detailed description
For elderly patients aged 75 years or older undergoing percutaneous coronary intervention with Onyx family drug-eluting stents, observe the safety and efficacy of transitioning from dual antiplatelet therapy to single therapy for one year after one month of dual antiplatelet therapy
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Onyx family | Safety and Efficacy of 1-Month DAPT in Elderly Patients at High Risk of Ischemia and Bleeding After Percutaneous Coronary Intervention with Onyx Family Stents |
Timeline
- Start date
- 2022-06-09
- Primary completion
- 2026-01-31
- Completion
- 2026-12-31
- First posted
- 2024-08-29
- Last updated
- 2024-09-19
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT06577896. Inclusion in this directory is not an endorsement.