Clinical Trials Directory

Trials / Completed

CompletedNCT00672516

Management of Bleeding Following Cardiopulmonary Bypass

Management of Excessive Bleeding Following Cardiopulmonary Bypass: A Pilot Feasibility Study

Status
Completed
Phase
Study type
Observational
Enrollment
43 (actual)
Sponsor
University of Minnesota · Academic / Other
Sex
All
Age
75 Years
Healthy volunteers
Not accepted

Summary

We believe ongoing bleeding during complex cardiac surgery can be accurately measured and that administration of a specific blood product replacement strategy designed to optimally slow or stop the bleeding can be followed by the during the operation. Patients at risk of significant bleeding after complex cardiac surgery will be approached to allow their operation to be watched by study personnel to see if ongoing blood loss can be accurately measured and to see how quickly a prescribed, standardized blood product replacement protocol to control the bleeding does slow or stop the bleeding. Permission to review the medical record to see if bleeding risk features can be identified and permission to follow the patient after surgery to see how they recover is also requested.

Conditions

Timeline

Start date
2008-04-01
Primary completion
2009-05-01
Completion
2009-05-01
First posted
2008-05-06
Last updated
2015-05-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00672516. Inclusion in this directory is not an endorsement.