Prevention of Radial Artery Occlusion: Prophylactic Hyperperfusion Evaluation Trial — PROPHET-II

Occlusion of Artery Clinical Trial

Official title:
Prevention of Radial Artery Occlusion: Prophylactic Hyperperfusion Evaluation Trial

Status Completed

Clinical Trial Summary

Evaluating the effect of ulnar artery compression while pressing on radial artery to stop bleeding, in maintaining radial artery potency, after cardiac catheterization through the radial artery. We prospectively plan to compare 3000 patients referred for cardiac catheterization, randomized into two groups, one group receiving radial artery compression for stopping bleeding, in a standard fashion following best practices, and the other group receiving radial artery compression using standard best practices and ulnar artery compression. Radial artery status will be evaluated in 24 hours and 30 days of the procedure to evaluate its potency, using plethysmography.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Occlusion of Artery

Clinical Trial Details

NCT number	NCT01564888
Study type	Interventional
Source	Total Cardiovascular Solutions
Contact
Status	Completed
Phase	Phase 4
Start date	January 2011
Completion date	July 2015

View Details

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