Trauma Clinical Trial - Optimal Fluid Resuscitation for Trauma Patients

Status Completed

Clinical Trial 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.

Clinical Trial 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. ;

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00527098
Study type	Observational
Source	University of Miami
Contact
Status	Completed
Phase	N/A
Start date	October 2007
Completion date	July 2010

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