Status:

COMPLETED

Centrifugation vs. Multiple-pass Hemofiltration of the Residual Cardiopulmonary Bypass Volume

Lead Sponsor:

University of Saskatchewan

Collaborating Sponsors:

Saskatoon Health Region

Conditions:

Coronary Artery Disease

Heart Valve Diseases

Eligibility:

All Genders

40-75 years

Phase:

NA

Brief Summary

Traditional cardiac surgery requires patient connection to the Cardiopulmonary Bypass (CPB) apparatus which takes over the function of the heart and lungs while the surgeon performs the necessary surg...

Detailed Description

This study is being performed because the traditional method of recovery of the residual volume of blood from the cardiopulmonary bypass circuit involves centrifugation and washing of whole blood with...

Eligibility Criteria

Inclusion

  • all males and females that will be receiving open heart surgery (Coronary Artery Bypass Grafts and / or Valve repair/replacement) during the study period.

Exclusion

  • history of bleeding disorders
  • history inflammatory diseases rheumatoid arthritis

Key Trial Info

Start Date :

March 1 2011

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 1 2012

Estimated Enrollment :

61 Patients enrolled

Trial Details

Trial ID

NCT01416792

Start Date

March 1 2011

End Date

October 1 2012

Last Update

April 1 2013

Active Locations (1)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

Royal University Hospital

Saskatoon, Saskatchewan, Canada, S7N 0W8