A prospective, multicentre, observational trial for hemodynamic reaction following initial fluid resuscitation in patients with hemorrhagic shock due to blunt trauma
Not Applicable
- Conditions
- Trauma patients with hemorrhagic shock
- Registration Number
- JPRN-UMIN000001059
- Lead Sponsor
- The General Planning Committee of Japanese Association for the Surgery of Trauma
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Penetrating trauma (2) When the physician selected permissive hypotension therapy (3) Cardiopulmonary arrest (4) Patients whose fluid therapy started before admission (5) Patients with terminal stage of chronic disease (6) When the physician consider that the initial fluid resuscitation therapy is inappropriate for the patient (state the specific reason)
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) Character of patients with hemorrhagic shock 2) Systolic blood pressure (SBP) and heart rate (HR) on admission 3) SBP and HR at the time when 1L of fluid replacement was administered. 4) SBP and HR at the time when 2L was administered. 5) SBP and HR at the time when the management of ER was finished. 6) Total volume of fluid replacement and blood transfusion at ER 7) Total volume of fluid replacement and blood transfusion during 24 hr 8) Details of interventional treatment performed for hemorrhage
- Secondary Outcome Measures
Name Time Method