N/A
N=119
Optimal Fluid Resuscitation for Trauma Patients
Trauma
Bottom Line
View on ClinicalTrials.gov: NCT00527098 ↗Enrolled (actual)
119
Serious AEs
0.0%
Results posted
May 2011
Primary outcome: Primary: Mortality — 0 participants
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Miami
- Primary completion
- Jul 2010
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Mortality |
— | — |
Summary
The purpose of this study is to determine if the overall fluid requirements for the first 24 hours after admission will be reduced with Hextend versus a standard of care crystalloid resuscitation fluid.
Eligibility Criteria
Inclusion Criteria
- Greater than or equal to 18 years old and less than 65 years old
- Admission with multi-system traumatic injury
- Admission to the intensive care unit
Exclusion Criteria
- Less than 18 or greater than 65 years old
- Pregnant or lactating
- No fluid resuscitation
Data sourced from ClinicalTrials.gov (NCT00527098). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.