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NCT00714766 Clinical Trial

Heat Stress and Volume Administration

Syncope Clinical Trial

Official title:
Heat Stress and Volume Administration

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00714766
Other study ID # Heat stress RH08
Secondary ID
Status Completed
Phase N/A
First received July 10, 2008
Last updated February 13, 2009
Start date July 2008
Est. completion date August 2008

Study information
Verified date February 2009
Source Rigshospitalet, Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

Heat stress reduces the central blood volume and causes orthostatic intolerance. The hypothesis is that infusion of volume may reduce effects of orthostatic stress during heat stress.

Recruitment information / eligibility
Status Completed
Enrollment 10
Est. completion date August 2008
Est. primary completion date August 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Age > 18 < 40

Exclusion Criteria:

- Abnormal medical history

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science

Related Conditions & MeSH terms

Intervention

Procedure:
• Intravascular volume administration
Infusion of colloid to reestablish CVP under heat stress

Locations
Country Name City State
Denmark Dept of anesthesiology 2041 Copenhagen

Sponsors (1)
Lead Sponsor Collaborator
Rigshospitalet, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome
Type Measure Description Time frame Safety issue
Primary Cardiac filling pressure in relation to cardiac SV with varying degress of lower body negative pressures No
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