the patients scheduled to open heart surgery
Conditions
Interventions
Sonoclot which evaluated blood coagulation and platelet function was used during operation. Observation was continued to the first day after operation
Control group was not used sonoclot. Observatio
Sponsors
Sapporo Medical University School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients whom scheduled or underwent cardiac surgery under cardiopulmonary bypass
Exclusion criteria
Exclusion criteria: Patients whom were unconscious or refused participation of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The amount of intraoperative transfusion after finished the cardiopulmonary bypass | — |
Countries
Japan
Contacts
Public ContactHiroshi Takeda
Sapporo Medical University School of Medicine Department of Anesthesiology
Outcome results
None listed