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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Different 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.