Heat Stress and Volume Administration

NCT ID: NCT00714766

Last Updated: 2009-02-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-07-31

Study Completion Date

2008-08-31

Brief Summary

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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.

Detailed Description

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Conditions

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Syncope

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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A

Group Type EXPERIMENTAL

Intravascular volume administration

Intervention Type PROCEDURE

Infusion of colloid to reestablish CVP under heat stress

Interventions

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Intravascular volume administration

Infusion of colloid to reestablish CVP under heat stress

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Age \> 18 \< 40

Exclusion Criteria

* Abnormal medical history
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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Rigshospitalet, Denmark

OTHER

Sponsor Role lead

Responsible Party

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Righospitale

Principal Investigators

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Niels Secher, MD, PhD

Role: STUDY_DIRECTOR

Rigshospitalet, Denmark

Locations

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Dept of anesthesiology 2041

Copenhagen, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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Heat stress RH08

Identifier Type: -

Identifier Source: org_study_id

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