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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01116609
Other study ID # Epi-perfusion
Secondary ID
Status Completed
Phase N/A
First received April 9, 2010
Last updated November 4, 2011
Start date October 2004
Est. completion date January 2010

Study information

Verified date November 2011
Source University of Aarhus
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

The purpose of this study is to define the local metabolic effects of epinephrine in the bilaterally perfused human leg.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date January 2010
Est. primary completion date November 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Male

Exclusion Criteria:

- Comorbidity

- Females

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Drug:
Epinephrine
unilateral leg infusion of Epinephrine 0.4 micrograms/m2/min

Locations

Country Name City State
Denmark Medical research laboratories, Aarhus University Hospital Aarhus

Sponsors (1)

Lead Sponsor Collaborator
University of Aarhus

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Arterio-Venous balances of metabolites Acute regional effect of epinephrine infusion in the femoral artery 6 hours infusion No
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