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Clinical Trials/NCT02034084
NCT02034084
Completed
Not Applicable

A Comparison of Left and Right Radial Approach for Percutaneous Coronary Procedures

Capital Medical University1 site in 1 country1,400 target enrollmentMarch 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Transradial Approach,
Sponsor
Capital Medical University
Enrollment
1400
Locations
1
Primary Endpoint
Total procedural duration
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Previous studies have shown that the transradial cardiac catheterization has decreased not only bleeding complications related to the access site and procedural discomfort but also morbidity and hospitalization as compared to transfemoral approach. At present, the right radial approach (RRA) is the first choice routinely for coronary angiography and interventions in daily clinical practice despite more marked subclavian artery tortuosity than left radial approach (LRA). Although LRA has been thought to be more direct access to the ascending aorta similar to transfemoral approach and may reduce fluoroscopy time and cerebrovascular complications compared with RRA, the application of LRA for coronary intervention is still low. Moreover, several studies have also obtained conflicting results showing no difference in procedural success rate compared LRA and RRA using Judkins catheters. To date, it remains unclear whether LRA is superior to RRA in term of safety and feasibility for coronary angiography and interventions in real world practice and few data of randomized control trial are available.

The aim of this study was to randomly investigate and compare the safety and feasibility of LRA compared with RRA for coronary diagnostic angiography in Chinese subjects.

The investigators will enroll consecutively for 2 years all patients undergoing coronary diagnostic procedures through trans radial approach.

The primary outcome was total procedural duration. Secondary outcomes included fluoroscopy time, dose of radiation including cumulative air kerma and dose area product, contrast volume and the incidence of vascular complications.

Registry
clinicaltrials.gov
Start Date
March 2011
End Date
June 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Capital Medical University
Responsible Party
Principal Investigator
Principal Investigator

Buxing Chen

Director of department of cardiology

Capital Medical University

Eligibility Criteria

Inclusion Criteria

  • All consecutive patients who undergo to diagnostic coronary procedures

Exclusion Criteria

  • Acute ST-elevation myocardial infarction
  • Previous coronary artery bypass graft surgery
  • Hemodynamic instability

Outcomes

Primary Outcomes

Total procedural duration

Time Frame: 1 day

Secondary Outcomes

  • Contrast volume(7 days)
  • Dose of radiation(7 days)
  • Fluoroscopy time(7 days)

Study Sites (1)

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