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Dehydroepiandrosterone (DHEA) replacement in patients with secondary adrenal insufficiency (hypopituitarism)

Dehydroepiandrosterone (DHEA) replacement in patients with secondary adrenal insufficiency (hypopituitarism)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14203656
Enrollment
20
Registered
2004-09-30
Start date
2002-12-01
Completion date
Unknown
Last updated
2020-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nutritional, Metabolic, Endocrine: Adrenal insufficiency Nutritional, Metabolic, Endocrine Adrenal insufficiency

Interventions

For the first 4 months each patient would receive either 50 mg of DHEA administered orally or a placebo tablet of identical appearance. Following a washout period of one month the form of therapy woul

Sponsors

Department of Health
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. 20 patients between the age of 20 and 60 years 2. With adrenal insufficiency secondary to panhypopituitarism of varying aetiology 3. Of at least one years duration enrolled from outpatient clinics of City General Hospital 4. They would be adequately replaced with regards to corticosteroid, thyroxine and sex steroid deficiency with unchanged replacement dose over the preceding 3 months 5. None of the patients would receive growth hormone replacement therapy 6. Patients with significant co-morbidity, those with hormone dependent conditions like breast cancer, pregnant women are excluded 7. Written consent would be obtained from all patients

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
1. Body mass index 2. Blood pressure (BP) 3. Quality of life (QoL) assessment 4. Hormone, Biochemical and Endothelial markers (detail give above) 5. Insulin tolerance test 6. Ultrasonographic assessment of endothelial function by checking carotid intima-media thickness 7. Flow mediated dilatation of the brachial artery

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026