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Thromboelastometry Guided Blood-Component Therapy After Cardiac Surgery: A Randomized Study

Not Applicable
Conditions
T81.0
D68.4
Haemorrhage and haematoma complicating a procedure, not elsewhere classified
Acquired coagulation factor deficiency
Registration Number
DRKS00017367
Lead Sponsor
Herzzentrum Universität Leipzig
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
104
Inclusion Criteria

• indication for cardiac surgery
• patient consent signed
• elective surgery
• age over 18 years
• persistent postoperative bleeding defined as drainage loss of 100 ml / 30 min or more than 200 ml / h after arrival at the intensive care unit

Exclusion Criteria

• patient with preoperatively known treatment-relevant coagulation disorder (haemophilia A / B, APC-resistance, factor XIII deficiency, HIT-II, etc.)
• pregnancy or breastfeeding

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary endpoints are transfusion requirements regarding red blood cells, platelets, plasma, fibrinogen or pooled factors.
Secondary Outcome Measures
NameTimeMethod
The secondary endpoints are 24-hour drainage loss, re-thoracotomy rate and cost analysis of blood and coagulation products.
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