Study to compare the outcomes of distal and proximal radial artery access used in coronary angioplasty
Not Applicable
- Conditions
- Health Condition 1: I20- Angina pectorisHealth Condition 2: I251- Atherosclerotic heart disease of native coronary arteryHealth Condition 3: I214- Non-ST elevation (NSTEMI) myocardial infarctionHealth Condition 4: I200- Unstable angina
- Registration Number
- CTRI/2023/07/055246
- Lead Sponsor
- Principal Investigator
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients are at least 18 years of age with palpable proximal and distal radial artery who are planned for percutaneous coronary intervention using 6F radial sheath and guiding catheter.
Exclusion Criteria
1.Patients having clinical instability with compromised hemodynamics.
2.ST segment elevation myocardial infarction undergoing primary PCI.
3.History of previous coronary angiography or PCI through trans-radial access.
4.Chronic kidney disease on maintenance hemodialysis.
5.Patient or family refusal
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary end point will be incidence of Radial Artery Occlusion at hospital discharge & at 60 daysTimepoint: At hospital discharge & at 60 days
- Secondary Outcome Measures
Name Time Method the secondary endpoints will include successful sheath insertion, access-site crossover, access site hematoma, access site bleeding, radial artery pseudoaneurysm, radial artery spasm during procedure, access site related pain according to visual analog scale.Timepoint: At hospital discharge & at 60 days