Hemostatic Compression Patterns After Transradial Coronary Intervention (HCPATRI)
Coronary Disease
About this trial
This is an interventional prevention trial for Coronary Disease focused on measuring Coronary Disease, Radial artery occlusion, transradial coronary intervention
Eligibility Criteria
Inclusion Criteria:
- Patients 18 years or older
- Patients who received TRI for the first time
Exclusion Criteria:
- Failure to puncture the radial artery in 1 attempt
- Inaccessible radial arteries because of anatomic variations, such as hypoplastic radial arteries and radioulnar loop, which can be confirmed by radial artery angiography before the TRI
- Patients who had previous radial procedure
- Patients who were receiving IIb/IIIa receptor antagonist treatment
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Other
Experimental
control group
experimental group
Participants allocated to the control group will receive a routine long term postoperative puncture site compression via TR Band. In control group, TR Band deflation is commenced at the 2nd hour with successive 5 mL air released at 2 hours intervals until the bladder was empty at the 6th hour, and the TR Band is removed at the 24th hour.
Participants allocated to the experimental group will receive a short term postoperative puncture site compression via TR Band. In experimental group, TR Band deflation is commenced at the 1st hour with 3 mL air released, and at the 2nd hour with 5ml, and at the 3rd hour with the remainder air in the bladder, and the TR Band is removed at the 12th hour.