Patients whom proposed massive hemorrhage during operation
Conditions
Interventions
Sonoclot group
Control group
Sponsors
Sapporo Medical University School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients aged 20 to 90 with ASA-physical status 1 to 4 whom proposed massive hemorrhage during operation
Exclusion criteria
Exclusion criteria: Patients whom were unconscious and refused the participation of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| total amount of fluid and transfusion during operation | — |
Secondary
| Measure | Time frame |
|---|---|
| total amount of hemorrhage during operation, the amount of transfusion and hemorrhage 24hr after operation, the correlation between the value of blood sample and that of blood coagulation and platelet function analyzer | — |
Countries
Japan
Contacts
Public ContactHiroshi Takeda
Sapporo Medical University School of Medicine Hospital Division
Outcome results
None listed