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
Location: See location...
Intervention Type: Device
Study Type: Observational
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.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Healthy Volunteers: f
View:
• Patients ≥ 19 years old
• Patients receiving Xience-Skypoint™ stents.
• The patient or guardian agrees to the study protocol and the schedule of clinical follow-up, and provides informed, written consent, as approved by the appropriate Institutional Review Board/Ethics Committee of the respective clinical site.
Locations
Other Locations
Republic of Korea
Asan Medical Hospital
RECRUITING
Seoul
Contact Information
Primary
Jung-hee Ham, Project manager
cvcrc5@amc.seoul.kr
82230104728
Time Frame
Start Date: 2023-12-14
Estimated Completion Date: 2026-02
Participants
Target number of participants: 2000
Treatments
XIENCE Skypoint™ stent
Patients receiving Xience-Skypoint™ stents
Related Therapeutic Areas
Sponsors
Leads: Seung-Jung Park
Collaborators: CardioVascular Research Foundation, Korea