Disruptions of the day-night rhythm after treatment for a non-functioning pituitary adenoma; a cross-sectional study using actigraphy.

Disruptions of the day-night rhythm after treatment for a non-functioning pituitary adenoma; a cross-sectional study using actigraphy. - Actigraphy in NFMA patients

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON39636

Enrollment

250

Registered

2012-12-06

Start date

2013-04-04

Completion date

Unknown

Last updated

2024-09-30

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

Conditions

Non-functioning pituitary adenoma non-hormone producing adenoma of the pituitary gland

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Informed consent Mentally competent Age 18-70 years NFMA patients: treated for non-functioning pituitary macroadenoma, adequate substitution of any hormone deficiencies for at least 4 months. Documented adenopituitary deficiencies. Hypocortisol patients: treatment for primary adrenal gland insufficiency or bilateral adrenalectomy, adequate substitution of cortisol for at least 4 months.

Exclusion criteria

Exclusion criteria: Pregnancy Diagnosted sleeping disorder Diseases of the hypothalamus or pituitary gland other that NFMA Chronic use of sleep medication or sedative medication Age >70 years

Design outcomes

Primary

Measure	Time frame
Registration of day-night rhythmicity and objective sleep duration using actigraphy and sleep diaries	—

Secondary

Measure	Time frame
Quality of life and subjective sleep quality	—

Countries

Netherlands

Outcome results