Intervention study about the additive infusion of concentrated fibrinogen preparation and the amount of blood transfusion for the massive hemorrhage case
Not Applicable
Recruiting
- Conditions
- Massive hemorrhage by trauma, gastrointestinal hemorrhage
- Registration Number
- JPRN-UMIN000019027
- Lead Sponsor
- Trauma and Acute Critical Care Medical Center,Medical Hospital,Tokyo Medical and Dental Universitiy
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Not provided
Exclusion Criteria
1.Pregnant woman 2.Under 20 years old 3.Immunocompromised (state) patients 4.Patients with allegy for blood products 5.Patients who are diagnosed as congenital low fibrinogen blood symptom 6.the patient that informed consent is not provided 7.the patient who is dead during primary care treatment even MTP procedure was exercised or not given the treatment with RCC,FFP and the concentrated fibrin preparation. 8.the patient who cannot perform a blood test after dosage
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The amount of total blood tranfusion until hemostasis completion
- Secondary Outcome Measures
Name Time Method