Traumatic Hemorrhagic Shock Patients
Conditions
Interventions
None listed
Sponsors
Kobe university
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Randomized controlled trial including more than 50% of patients with traumatic hemorrhagic shock
Exclusion criteria
Exclusion criteria: Conference abstract Language other than English
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional Outcome | — |
Secondary
| Measure | Time frame |
|---|---|
| Adverse Event Total Blood Product Usage ICU Length of Stay Hospital Length of Stay Short-term Mortality Long-term Mortality | — |
Countries
Japan
Contacts
Public ContactNobuto Nakanishi
Kobe University Graduate School of Medicine Division of Disaster and Emergency Medicine, Department of Surgery Related
Outcome results
None listed