Evaluation of Effectiveness and Safety of Coroflex ISAR NEO Stent in Routine Clinical Practice; A Multicenter, Prospective Observational Study
Status: Recruiting
Location: See all (11) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY
The objective of this study is to evaluate the effectiveness and safety of Coroflex ISAR NEO 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 Coroflex ISAR NEO 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
Bucheon Sejong Hospital
NOT_YET_RECRUITING
Bucheon-si
The Catholic Univ. of Korea BUCHEON ST.Mary's hospital
NOT_YET_RECRUITING
Bucheon-si
Veterans Hospital
RECRUITING
Daegu
Chonnam National University Hospital
NOT_YET_RECRUITING
Gwangju
Inje University Ilsan Paik Hospital
NOT_YET_RECRUITING
Ilsan
Myongji Hospital
NOT_YET_RECRUITING
Ilsan
Sejong Chungnam National University Hospital
RECRUITING
Sejong
Asan Medical Center
RECRUITING
Seoul
Seoul National University Boramae Medical Center
NOT_YET_RECRUITING
Seoul
The Catholic university of Korea, ST. Vincent's Hospital
RECRUITING
Suwon
Uijeongbu Eulji Medical Center
WITHDRAWN
Uijeongbu-si
Contact Information
Primary
Jung-Hee Ham, Project manager
cvcrc5@amc.seoul.kr
82230104728
Time Frame
Start Date: 2025-01-09
Estimated Completion Date: 2030-12-31
Participants
Target number of participants: 1000
Treatments
Coroflex ISAR NEO
Patients receiving percutaneous coronary intervention with Coroflex ISAR NEO stents
Related Therapeutic Areas
Sponsors
Collaborators: The CardioVascular Research Foundation (CVRF)
Leads: Seung-Jung Park