Six Months DHEA Treatment in Female Adrenal Failure

NCT ID: NCT00471900

Last Updated: 2007-05-10

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

2001-10-31

Study Completion Date

2003-02-28

Brief Summary

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DHEA is an adrenal deriven androgen precourser. The impact of DHEA substitution therapy in adrenal failure is unknown as well as the physiologically effects of DHEA is unknown. Effects of physiologically DHEA substitution is investigated in the model of female adrenal failure.

Detailed Description

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Conditions

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Adrenal Insufficiency

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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dehydroepiandrosterone (DHEA)

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Female,
* Adrenal insuficiency,
* Stable and safe anticonception,
* Stable hydrocortison substituation treatment.

Exclusion Criteria

* Neoplastic and thromboembolic disease,
* Diabetes mellitus.
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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University of Aarhus

OTHER

Sponsor Role lead

Principal Investigators

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Jens S Christiansen, Professor

Role: STUDY_DIRECTOR

Medical Dept. M, Aarhus University Hospital

Other Identifiers

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200110130

Identifier Type: -

Identifier Source: org_study_id