The patients who are planned to undergone open heart surgery
Conditions
Interventions
The patients who are planned to perform Sonoclot guided blood transfusion This study will be examined from preoperative days to the first postoperative day.
The patients who are planned to perf
Sponsors
Sapporo Medical University School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: The patients who are planned to perform open heart surgery.
Exclusion criteria
Exclusion criteria: The patients who are difficult of mutual understanding and not be obtained consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the numbers of order of fresh frozen products and platelets, and the amount of blood transfusion of that | — |
Countries
Japan
Contacts
Public ContactAsami Nakano
Sapporo Medical University School of Medicine clinical study section of secretariat
Outcome results
None listed