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Rapid Clamp Release Post Trans-radial Cardiac Catheterization

Not Applicable
Completed
Conditions
Cardiac Catheterization
Interventions
Other: Compression clamp release
Registration Number
NCT03645837
Lead Sponsor
Lawson Health Research Institute
Brief Summary

The purpose of the study is to compare different short durations of radial clamp application following an angiogram via a trans-radial approach.

Detailed Description

This is a single-center, prospective, randomized study that will enroll patients that are referred for an angiogram and will compare 3 different durations of radial clamp applications. Patients will be randomly assigned to either 10, 20 or 30-minute clamp applications. The clamps will be gradually released at the end of the assigned durations and participants will be assessed for the radial artery occlusion, hematoma, and other bleeding events.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
450
Inclusion Criteria
  1. Diagnostic catheterization
  2. 5 F slender sheath
  3. Normal ulno-palmar circulation
Exclusion Criteria
  1. Abnormal ulno-palmar circulation type D
  2. Ad hoc percutaneous coronary intervention
  3. Heparin or other anticoagulation

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
10 minutesCompression clamp releaseCompression clamp release start after 10 minutes
20 minutesCompression clamp releaseCompression clamp release start after 20 minutes
30 minutesCompression clamp releaseCompression clamp release start after 30 minutes
Primary Outcome Measures
NameTimeMethod
Hematoma1 hour

Hematoma larger than 5 cm

Radial artery occlusion1 hour

Assessed by Doppler

Secondary Outcome Measures
NameTimeMethod
Bleeding - any1 hour

Minor hematoma

Trial Locations

Locations (1)

London Health Sciences Centre

🇨🇦

London, Ontario, Canada

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