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)
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1
Royal University Hospital
Saskatoon, Saskatchewan, Canada, S7N 0W8