NL-OMON27592Not yet recruitingNot Applicable
Target Activated Clotting time for anticoagulation during cardiopulmonary bypass
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Enrollment
- 1,536
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •Patients scheduled for elective CABG or cardiac valve surgery, or a combination of CABG with valve surgery, or (cross-clamped) aortic root or ascendens procedures with cardiopulmonary bypass.
- •Adult surgery
- •Informed consent
Exclusion Criteria
- •Re-operations
- •Aorta surgery (requiring SCP and/or circulatory arrest)
- •Emergency operation
- •Minimized extracorporeal circuits (MECC)
- •Deep hypothermia (<32oC)
- •Patients with congenital coagulation factor abnormalities (e.g. von Willebrand disease, hemophilia)
- •Patients with acquired coagulation factor abnormalities (e.g. acquired haemophilia, acquired von Willebrand disease, haematological malignities, thrombocytopenia <75*109/L)
- •Patients with anemia (hemoglobin value < 6.5 mmol/l)
Investigators
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