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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00197847
Other study ID # KA 02071
Secondary ID
Status Active, not recruiting
Phase N/A
First received September 12, 2005
Last updated September 12, 2005
Start date December 2002
Est. completion date September 2005

Study information

Verified date September 2005
Source Herlev Hospital
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Observational

Clinical Trial Summary

Purpose of the study is to investigate and quantify known and possible new riskfactors for nosocomiel infection and death in the intensive care setting.

As new riskfactors Mannose Binding Lechtin and Procalcitonin are chosen and compared to established riskfactors.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 549
Est. completion date September 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:Admission to ICU -

Exclusion Criteria:Absence of informed consent and age less than 18 years

Study Design

Observational Model: Defined Population, Time Perspective: Longitudinal


Locations

Country Name City State
Denmark Department of Intensive Care Copenhagen Copenhagen Couty

Sponsors (1)

Lead Sponsor Collaborator
Herlev Hospital

Country where clinical trial is conducted

Denmark, 

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