MedTrace Logo

Preemptive Resuscitation for Eradication of Septic Shock

NCT01449721 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 142

Last updated 2017-10-04

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to assess the ability of an empiric resuscitation strategy compared to standard care to decrease the incidence of organ failure in normotensive sepsis patients.

Conditions

Interventions

DRUG

Intravenous fluid

0.9% Sodium chloride intravenous fluid

Sponsors & Collaborators

  • Christiana Care Health Services

    lead OTHER

Principal Investigators

  • Alan Jones, MD · University of Mississippi Medical Center

  • Ryan Arnold, MD · Cooper University Hospital: Cooper Medical School of Rowan University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-09-30
Primary Completion
2015-01-31
Completion
2016-01-31

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 NCT01449721 on ClinicalTrials.gov