MedTrace Logo

Saline Against Lactated Ringers or Plasmalyte in the Emergency Department

NCT02614040 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14000

Last updated 2017-09-15

No results posted yet for this study

Summary

This study will be a cluster-randomized, single-center trial comparing 0.9% saline (normal saline) vs physiologically-balanced crystalloid fluids (Lactated Ringers or Plasmalyte A) for intravenous fluid administration in the emergency department.

Conditions

Interventions

OTHER

0.9% Saline

0.9% Saline will be used whenever an isotonic crystalloid is ordered

OTHER

Physiologically-balanced isotonic crystalloid

Lactated Ringers or Plasma-Lyte© A will be used whenever an isotonic crystalloid is ordered

Sponsors & Collaborators

  • Vanderbilt University

    lead OTHER

Principal Investigators

  • Wesley Self, MD MPH · Vanderbilt University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-01
Primary Completion
2017-06-30
Completion
2017-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT02614040 on ClinicalTrials.gov