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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00197899
Other study ID # KA 04015
Secondary ID
Status Active, not recruiting
Phase N/A
First received September 13, 2005
Last updated December 12, 2005
Start date March 2004
Est. completion date January 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 Interventional

Clinical Trial Summary

The purpuse of this study is to examine the acute phase respons when different doses of E. Coli Endotoxin is injected in healty volunters.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 0
Est. completion date January 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: Healty volunteers -

Exclusion Criteria:

Infection 14 days prior to the trial Regular medication Present and /or former heart disease -

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Drug:
E. Coli endotoxin


Locations

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

Sponsors (1)

Lead Sponsor Collaborator
Herlev Hospital

Country where clinical trial is conducted

Denmark, 

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