Safety and Efficacy of Procalcitonin Guided Antibiotic Therapy in Adult Intensive Care Units (ICU's)

NCT01139489 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1575

Last updated 2016-01-06

No results posted yet for this study

Summary

This is a randomized controlled trial comparing standard-of-care therapy of infections in critically ill patients with a procalcitonin-guided approach evaluating efficacy (antibiotics consumption) and safety (mortality).

Conditions

  • Sepsis
  • Severe Sepsis
  • Septic Shock

Interventions

OTHER

procalcitonin-guidance

If procalcitonin levels decrease to predefined levels, antibiotic therapy will be discontinued.

Sponsors & Collaborators

  • UMC Utrecht

    collaborator OTHER
  • Elisabeth-TweeSteden Ziekenhuis

    collaborator OTHER
  • Diakonessenhuis, Utrecht

    collaborator OTHER
  • Isala

    collaborator OTHER
  • Atrium Medical Center

    collaborator OTHER
  • Dijklander Ziekenhuis

    collaborator OTHER
  • Bronovo Hospital

    collaborator OTHER
  • Medical Center Haaglanden

    collaborator OTHER
  • Slotervaart Hospital

    collaborator OTHER
  • University of Groningen

    collaborator OTHER
  • Martini Hospital Groningen

    collaborator OTHER
  • Canisius-Wilhelmina Hospital

    collaborator OTHER
  • Medisch Spectrum Twente

    collaborator OTHER
  • St. Lucas Andreas Ziekenhuis Hospital

    collaborator OTHER
  • Amsterdam UMC, location VUmc

    lead OTHER

Principal Investigators

  • Evelien de Jong, MSc · Amsterdam UMC, location VUmc

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-11-30
Primary Completion
2014-08-31
Completion
2014-08-31

Countries

  • Netherlands

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 NCT01139489 on ClinicalTrials.gov