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Effects of Corticotropin Releasing Hormone (CRH) on the Sleep in Patients With Hypopituitarism

Effects of CRH on the Sleep in Patients With Hypopituitarism

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00666068
Enrollment
30
Registered
2008-04-24
Start date
2008-02-29
Completion date
2008-12-31
Last updated
2011-05-12

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

Conditions

Hypopituitarism

Keywords

Patients with hypopituitarism

Brief summary

In contrast to healthy subjects, patients with hypopituitarism do not exhibit endocrine responses when hormones are injected. This is at least true for those with a complete insufficiency of the anterior pituitary. For example, administration of corticotropin releasing hormone (CRH) is not followed by an increase of ACTH and cortisol. Therefore, pure hormone effects can be investigated. It is well established that hormones of the hypothalamic-pituitary-adrenal axis are involved in sleep regulation. In rodents, CRH decreased slow wave sleep (SWS). In humans, CRH was reported to increase wakefulness and to decrease SWS and REM sleep. Primary objective was therefore to study the effect of CRH on patients with hypopituitarism. To date, there is no information on sleep of patients with hypopituitarism. Secondary objective is therefore to compare sleep of patients with hypopituitarism with sleep of age-matched healthy controls.

Interventions

OTHERcorticotropin releasing hormone (CRH)

50 µg injected at 2200, 2300, 0000, and 0100

OTHERPlacebo

injected at 2200, 2300, 0000, and 0100

Sponsors

Max-Planck-Institute of Psychiatry
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

Patients with hypopituitarism Inclusion Criteria: * Age 18-75 years * Complete insufficiency of the anterior pituitary * Stable hormone substitution for at least 3 months

Exclusion criteria

* Hormone excess in the past * Sleep disorder, e.g. sleep apnea syndrome Healthy controls Inclusion Criteria: * Age 18-75 years

Design outcomes

Primary

MeasureTime frame
Sleep-EEG variables, conventionally and quantitatively analyzedwithin the first month

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026