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Clinical Trials/NL-OMON27592
NL-OMON27592Not yet recruitingNot Applicable

Target Activated Clotting time for anticoagulation during cardiopulmonary bypass

niversity Medical Center Utrecht0 sites1,536 target enrollmentStarted: TBDLast updated:

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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