Status:
TERMINATED
The Study for Evaluate of Satety and Dfficacy of Hemostatic Device
Lead Sponsor:
Pusan National University Yangsan Hospital
Conditions:
Coronary Artery Disease
Eligibility:
All Genders
20-99 years
Phase:
NA
Brief Summary
The goal of this clinical trial is to compare the new pneumatic compression device TRAcelet with conventional compression method in patients undergone transradial coronary angiography. The main questi...
Detailed Description
Although there are several devices available for radial artery hemostasis, conventional compression with a gauze pad is thought to be the easiest method. One of the devices with a pneumatic compressio...
Eligibility Criteria
Inclusion
- aged over 20 years
- Underwent coronary angiography under suspicion of coronary artery disease
- Agreed to participate in the trial before the coronary angiography procedure
Exclusion
- Bleeding tendency due to congenital or acquired disorders such as severe liver disease, thrombocytopenia (platelet count below 50,000 cells/μL)
- Those who were on anticoagulants.
- Patients who could not provide voluntary consent.
Key Trial Info
Start Date :
December 14 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 31 2021
Estimated Enrollment :
227 Patients enrolled
Trial Details
Trial ID
NCT06590571
Start Date
December 14 2018
End Date
December 31 2021
Last Update
September 19 2024
Active Locations (1)
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1
Pusan National University Yangsan Hospital
Yangsan, Gyeongsannam-do, South Korea, 50612