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Clinical Trials/NCT00527098
NCT00527098
Completed
N/A

Optimal Fluid Resuscitation for Trauma Patients

University of Miami1 site in 1 country119 target enrollmentOctober 2007
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ConditionsTrauma

Overview

Phase
N/A
Intervention
Not specified
Conditions
Trauma
Sponsor
University of Miami
Enrollment
119
Locations
1
Primary Endpoint
Mortality
Status
Completed
Last Updated
13 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief 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.

Detailed Description

Following severe multi-system traumatic injury, the first 24 hours of standard resuscitation fluid will be either Hextend or crystalloid depending upon attending preference. No tests or interventions will be performed for research purposes. Data will be collected prospectively from patient medical records and attending clinicians to monitor fluid requirements, hemodynamics and outcome.

Registry
clinicaltrials.gov
Start Date
October 2007
End Date
July 2010
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kenneth Proctor

Professor

University of Miami

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

Outcomes

Primary Outcomes

Mortality

Time Frame: From hospital arrival up to an average of 3.5 weeks

Study Sites (1)

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