Evaluation of Effectiveness and Safety of Drug-Eluting Balloon in Routine Clinical Practice; A Multicenter Prospective Observational Cohort Study

Status: Recruiting
Location: See all (8) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY

The purpose of this study is to evaluate long-term effectiveness and safety of patients with coronary disease treated with drug eluting balloon in real world practice.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 20
Healthy Volunteers: f
View:

• After pre dilatation residual stenosis 30% and less and also without vessel dissection interrupted blood flow

• Age 20 and more

• Treated with Balloon angioplasty

• Signed informed consent and agreed to follow protocol

Locations
Other Locations
Republic of Korea
Soon Chun Hyang University Hospital Bucheon
TERMINATED
Bucheon-si
Keimyung University Dongsan Medical Center
RECRUITING
Daegu
The Catholic University of Korea, Daejeon ST. Mary's Hospital
TERMINATED
Daejeon
Dong-A Medical Center
RECRUITING
Pusan
Asan Medical Center
RECRUITING
Seoul
Gangnam Severance Hospital
RECRUITING
Seoul
Korea University Guro Hospital
RECRUITING
Seoul
Ulsan University Hospital
TERMINATED
Ulsan
Time Frame
Start Date: 2014-01
Estimated Completion Date: 2028-06
Participants
Target number of participants: 1500
Treatments
Patients with coronary artery disease
Authors
Related Therapeutic Areas
Sponsors
Collaborators: B. Braun Korea Co., Ltd., CardioVascular Research Foundation, Korea
Leads: Seung-Jung Park

This content was sourced from clinicaltrials.gov