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Normal Saline Versus Plasmalyte in Initial Resuscitation of Trauma Patients

NCT01270854 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 46

Last updated 2017-05-30

No results posted yet for this study

Summary

The purpose of this study is to determine whether an intravenous salt solution called "Plasmalyte" causes less abnormality of the body's acid levels than a solution called "Normal Saline."

Conditions

  • Wounds and Injuries
  • Multiple Trauma
  • Disorder of Fluid Balance

Interventions

OTHER

Plasmalyte A

Intravenous fluid

OTHER

Normal Saline

Intravenous fluid

Sponsors & Collaborators

  • Bayer

    collaborator INDUSTRY

  • University of California, Davis

    lead OTHER

Principal Investigators

  • Garth H. Utter, MD · University of California, Davis

  • Lynette A. Scherer, MD · University of California, Davis

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-02-28
Primary Completion
2012-02-29
Completion
2012-04-30

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01270854 on ClinicalTrials.gov