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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00144638
Date of registration: 01/09/2005
Primary sponsor: Danish Procalcitonin Study Group
Public title: Procalcitonin Increase Identifies Critically Ill Patients at High Risk of Mortality
Scientific title: Procalcitonin Increase Identifies Critically Ill Patients at High Risk of Mortality
Date of first enrolment: January 2002
Target sample size: 450
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT00144638
Study type:  Observational
Study design:  Observational Model: Defined Population, Observational Model: Natural History, Time Perspective: Longitudinal, Time Perspective: Prospective  
Countries of recruitment
Denmark
Contacts
Name:   Lars Heslet, MD, MD.Sc.
Address: 
Telephone:
Email:
Affiliation:  Dept. 4131, Rigshospitalet, Blegdamsvej 9, DK-2100
Key inclusion & exclusion criteria

Inclusion Criteria: Admitted to the ICU 4131 of Rigshospitalet Copenhagen University
Hospital in the year 2002

-

Exclusion Criteria:

Recent (< 3 months) liver transplantation

Expected admission < 24 h



Age minimum: N/A
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Sepsis - to Reduce Mortality in the Intensive Care Unit
Intervention(s)
Primary Outcome(s)
Secondary Outcome(s)
Secondary ID(s)
DPSG1
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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