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Prevention of Radial Artery Occlusion: Prophylactic Hyperperfusion Evaluation Trial

NCT01564888 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 3000

Last updated 2019-09-17

No results posted yet for this study

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.

Conditions

  • Occlusion of Artery

Interventions

PROCEDURE

Ulnar artery compression

Compression of ulnar artery for 2 hours with radial artery hemostasis

Sponsors & Collaborators

  • Total Cardiovascular Solutions

    lead OTHER

Principal Investigators

  • Samir B Pancholy, MD

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2015-07-31
Completion
2015-07-31

Countries

  • Czechia
  • India

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01564888 on ClinicalTrials.gov