RecruitingNot ApplicableNCT03204357

Fresh Autologous Whole Blood Transfusion After Cardiopulmonary Bypass

Targeted Fresh Autologous Whole Blood Transfusion After Cardiopulmonary Bypass: a Prospective Randomized Controlled Trial.


Sponsor

University of Colorado, Denver

Enrollment

70 participants

Start Date

Jan 24, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 YearsMax Age: 90 Years

Inclusion Criteria4

  • Adult subjects aged 18 to 90
  • Able to provide informed consent
  • Willing to accept autologous or allogenic blood transfusion
  • Scheduled for elective cardiac surgery with cardiopulmonary bypass

Exclusion Criteria4

  • Pre-operative administration of allogenic blood bank products in the previous 3 months
  • Hemodynamically unstable defined as a systolic blood pressure less than 90 mmHg with a heart rate greater 100 or requiring intravenous vasopressor medications
  • Significant active infection or sepsis defined by positive blood culture or positive wound culture
  • Hemoglobin less than 7 g/dl

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Interventions

OTHERFresh Autologous whole Blood

Subjects randomized this arm will receive fresh autologous whole blood

OTHERStandard of Care Expectant management of bleeding

the control group that will receive the standard of care expectant management of bleeding and transfusion of allogenic banked blood products


Locations(1)

University of Colorado Hospital

Aurora, Colorado, United States

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NCT03204357


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