Clinical Trials Directory

Trials / Terminated

TerminatedNCT00364494

Hemodilution and Outcome in Cardiac Surgery

Effect of Moderate Hemodilution During Cardiopulmonary Bypass on Postoperative Outcome Following Cardiac Surgery

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
Sponsor
Università Vita-Salute San Raffaele · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

An hematocrit of 21-25% is supposed to perform the best organ protection during cardiopulmonary bypass for cardiac surgery. The investigators want to establish the best timing for a transfusion (in patients with a predicted low hematocrit during cardiopulmonary bypass) and the efficacy of preprocedural hemodilution (in patients with a predicted high hematocrit during cardiopulmonary bypass) in patients undergoing cardiac surgery.

Conditions

Interventions

TypeNameDescription
PROCEDUREDifferent timing of red blood cells transfusion (substudy 1); Acute hemodilution versus no hemodilution (substudy 2)Subgroup 1,with Ht\<21% receive an hemotransfusion before or after CEC;subgroup 2,with Ht\>25% bleed or not

Timeline

Start date
2006-11-01
Primary completion
2007-04-01
Completion
2007-04-01
First posted
2006-08-15
Last updated
2009-08-14

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT00364494. Inclusion in this directory is not an endorsement.