Redon drain blood quality before and after cell saver processing during CABG procedures: a pilot study
Recruiting
- Conditions
- autotransfusion10011082transfusion with own blood
- Registration Number
- NL-OMON49048
- Lead Sponsor
- niversitair Medisch Centrum Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
Scheduled for elective CABG with the use of saphenous vein graft material
Age >=18 years
Capable of understanding and speaking Dutch.
Exclusion Criteria
Hematologic disorders
Sepsis
Unable to correctly understand the research by means of different langue
barrier or mental impairment
Less than 50 ml of blood has been collected in the redon drain at the end of
the surgery
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Blood rheology</p><br>
- Secondary Outcome Measures
Name Time Method <p>Blood gas parameters<br /><br>Baseline platelet activation and activation triggered by a receptor activator<br /><br>Inflammatory markers: Interleukin -6 (CXCL6), Interleukin -8 (CXCL8) and tumor<br /><br>necrosis factor-a (TNF-a)<br /><br>Hemolysis index</p><br>