Optimal Fluid Resuscitation for Trauma Patients

Completed

Conditions studied: Trauma

In brief

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.

Key facts

Study ID

NCT00527098

Run by

University of Miami

People needed

119

Starts

2007-10-01

Expected to finish

2010-07-01

Last updated by the study team

2013-02-22

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• Less than 18 or greater than 65 years old
• Pregnant or lactating
• No fluid resuscitation

Where it is running

• Ryder Trauma Center — Miami, Florida, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.