Heparin vs Placebo for Cardiac Catheterization

Status Recruiting

Clinical Trial Summary

Patients undergoing cardiac catheterization will be randomized to 3 groups: no anticoagulant, low dose anticoagulant and high dose anticoagulant.

Clinical Trial Description

Patients undergoing diagnostic cardiac catheterization via the trans-radial approach will be randomly allocated (1:1:1) to receive either low-dose UFH (25 IU/Kg -maximal dose 3,000 IU), high-dose UFH 50 IU/kg -maximal dose 5,000 IU) or N/S 0.9%. After 30 minutes, patients will undergo a gradual wrist band release. Hematoma and radial artery occlusion will be assessed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04374799
Study type	Interventional
Source	Lawson Health Research Institute
Contact	Shahar Lavi, MD
Phone	519-6633611
Email	Shahar.lavi@lhsc.on.ca
Status	Recruiting
Phase	Phase 3
Start date	October 5, 2020
Completion date	December 2025

View Details

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