Microcirculation Guided Therapy Versus "Standard Treatment" of Severe Sepsis

NCT00484133 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2008-01-22

No results posted yet for this study

Summary

The purpose of this study is to asses the recovery of organ failure between two resuscitation protocols in severe sepsis: standard, pressure guided therapy versus a microcirculation guided therapy

Conditions

  • Severe Sepsis
  • Microcirculation

Interventions

DRUG

Dopamine

DRUG

dobutamine

DRUG

enoximone

DRUG

nitroglycerine

DRUG

noradrenaline

Sponsors & Collaborators

  • Onze Lieve Vrouwe Gasthuis

    lead OTHER

Principal Investigators

  • Rutger v Raalte, MD · Onze Lieve Vrouwe Gasthuis, intensive care unit

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-06-30
Primary Completion
2008-12-31

Countries

  • Netherlands

Study Locations

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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 NCT00484133 on ClinicalTrials.gov