Comparison of two devices for the viscoelastic, point-of-care assessment of hemostasis in cardiac surgery.
Recruiting
- Conditions
- Perioperative coagulation disorder
- Registration Number
- DRKS00014153
- Lead Sponsor
- niversitätsklinikum Essen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 25
Inclusion Criteria
Cardio-pulmonary-bypass surgery
Exclusion Criteria
preoperative anemia
complex procedures
hereditary coagulation disorders,
intake of direct oral anticoagulants or dual anti platelet therapy within 3 days prior to inclusion
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment of correlation, and agreement (Bland-Altman-Analyses and Cohens Kappa) of corresponding coagulation times, clot firmness values, and lysis parameters from the two different devices.
- Secondary Outcome Measures
Name Time Method