Fresh Autologous Whole Blood Transfusion After Cardiopulmonary Bypass
Recruiting
N/A
Interventional Study
Cardiac Disease
Bleeding Postoperative
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 90
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 70 (estimated)
- Sponsor
- University of Colorado, Denver · Other
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About This Trial
Autologous blood transfused at the end of cardiopulmonary bypass will reduce total blood loss 24 hours after surgery and improve mitochondrial oxygen delivery measured by plasma succinate levels. The study design is a prospective randomized interventional trial of transfusion of fresh autologous whole blood versus standard of care expectant management of bleeding during elective cardiac surgery.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Adult subjects aged 18 to 90
2. Able to provide informed consent
3. Willing to accept autologous or allogenic blood transfusion
4. Scheduled for elective cardiac surgery with cardiopulmonary bypass
Exclusion Criteria:
1. Pre-operative administration of allogenic blood bank …
Contacts