Trials / Recruiting
RecruitingNCT05981911
Evaluation of Effectiveness and Safety of Xience Skypoint Stents in Routine Clinical Practice
a Non-randomized, Prospective, Open-label Registry to Compare the Effectiveness and Safety of XIENCE Skypoint™ Stents Versus Other DESs in Patients With Coronary Artery Disease
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 2,000 (estimated)
- Sponsor
- Seung-Jung Park · Academic / Other
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to evaluate the effectiveness and safety of XIENCE Skypoint stents in comparison to other drug-eluting stents (DES) in real-world practice.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | XIENCE Skypoint™ stent | Percutaneous coronary intervention with Xience-Skypoint™ stent |
Timeline
- Start date
- 2023-12-14
- Primary completion
- 2026-06-01
- Completion
- 2026-12-01
- First posted
- 2023-08-08
- Last updated
- 2026-01-02
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT05981911. Inclusion in this directory is not an endorsement.