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Clinical Trials/NCT01021631
NCT01021631
Unknown
Phase 3

Transfusion Requirements After Cardiac Surgery: a Randomized Controlled Clinical Trial (TRACS STUDY)

Instituto do Coracao1 site in 1 country500 target enrollmentFebruary 2009
ConditionsCardiac Surgery

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Cardiac Surgery
Sponsor
Instituto do Coracao
Enrollment
500
Locations
1
Primary Endpoint
The primary purpose of this study is to compare clinical outcomes after cardiac surgery in patients submitted to different strategies of red blood cell transfusion
Last Updated
16 years ago

Overview

Brief Summary

Blood transfusion is related to worse outcomes and the triggers for red blood cells transfusion are not well defined in cardiac surgery. Retrospective studies in cardiac surgery do not show benefits of red blood cell transfusion in reduction of morbidity and mortality in cardiac surgery. There are no prospective studies comparing outcomes between restrictive or liberal strategy in cardiac surgery.This study is a double-blind randomized study comparing clinical outcomes between two strategies of transfusion in cardiac surgery - liberal or restrictive.

Detailed Description

Blood transfusion is commonly performed in patients submitted to cardiac surgery. However, there are many studies reporting adverse effects of this intervention and final data on benefits are not available. There are no prospective studies in cardiac surgery regarding red blood cell transfusions requirements. There are retrospective studies in cardiac surgery suggesting worse outcomes including higher rates of mortality in patients submitted to red blood transfusion. Hematocrit levels around 30% are usually recommended not evidence based. Our purpose is to prospectively evaluate two strategies of transfusion in 500 patients submitted to elective cardiac surgery: a liberal strategy - patients receive blood transfusion when hematocrit is lower than 30% since the intraoperative period until the ICU discharge; a restrictive strategy - patients receive blood transfusion only when hematocrit is lower than 24%. Clinical outcomes, costs and quality of life will be compared.

Registry
clinicaltrials.gov
Start Date
February 2009
End Date
April 2010
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • All elective primary and redo adult cardiac surgical patients for coronary artery bypass grafting, valve procedure or combined procedures
  • Adults patients
  • Written informed consent

Exclusion Criteria

  • Age less than 18 years
  • Transplant procedures
  • Emergency procedures
  • Aortic repairs
  • Congenital procedures
  • Previous anemia (hemoglobin lower than 10 g/dL)
  • Previous thrombocytopenia (platelet number lower than 100.000/mm3)
  • Previous known coagulopathy
  • Pregnancy
  • Those unable to receive blood transfusion

Outcomes

Primary Outcomes

The primary purpose of this study is to compare clinical outcomes after cardiac surgery in patients submitted to different strategies of red blood cell transfusion

Time Frame: 30 days after surgery

Secondary Outcomes

  • To compare length of stay in ICU, length of stay in Hospital, health-related quality of life, hospital costs and mortality between groups.(3 months)

Study Sites (1)

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