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Retransfusion or Not of Cardiotomy Blood

Not Applicable
Conditions
Blood Loss, Surgical
Registration Number
NCT04574128
Lead Sponsor
Örebro University, Sweden
Brief Summary

This randomised controlled trial has a non-inferiority design. The aim is to test if the blood loss (volume in mL and hemoglobin) is effected by heart and lung cardiotomy retransfusion, or not? Forty CABG (Coronary Artery By pass Grafting) patients will be allocated to either receive retransfusion (n=20) of cardiotomy blood via the heart and lung mashine, or no retransfusion (n=20).

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Elective CABG.
Exclusion Criteria
  • Anaemia, infection, massive bleeding, CABG off pump.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Primary Outcome Measures
NameTimeMethod
blood lossDuring 5 days hemoglobin will be measured as the clinical rutine or as needed.

Hemoglobin

Blood lossDuring 2 days or while surgical drains remains, blood volume in mL is measured.

Blood volume in millilitre (mL)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University Hospital in Örebro

🇸🇪

Örebro, Sweden

University Hospital in Örebro
🇸🇪Örebro, Sweden
Camilla Wistrand, PhD
Contact
+46707686938
camilla.wistrand@regionorebrolan.se

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