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Completed

NCT Number: NCT02096510

Ultradian Subcutaneous Hydrocortisone Infusion in Addison Disease and Congenital Adrenal Hyperplasia

The aim of this study is to compare the effects of tablet treatment, circadian and combined circadian and ultradian subcutaneous hydrocortisone infusion on steroid metabolism and tissue responses to therapy.

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Key information

About this study

The conventional glucocorticoid replacement therapy in primary adrenal insufficiency (Addison's disease) and congenital adrenal hyperplasia renders the cortisol levels unphysiological, which may cause symptoms and long-term complications. This therapeutical approach does not enable to restore physiological circadian and ultradian rhythm of glucocorticoids. Current studies conclude that constant or unphysiological administration of glucocorticoids leads to abnormal gene transcription and causes sides effect of glucocorticoids treatment and long standing complications Glucocorticoid replacement is technically feasible by continuous subcutaneous hydrocortisone infusion, which can mimic not only the normal diurnal cortisol rhythm, but potentially also the ultradian cadence.

This is a pilot trial with an open cross-over design of 3 x minimum 2 weeks in 10 patients comparing the effects of tablet treatment versus continuous subcutaneous hydrocortisone infusion versus ultradian subcutaneous hydrocortisone infusion on serum, salivary, tissue hormonal response and glucocorticoid related gene expression.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • clinical diagnosis of primary adrenal insufficiency
  • Written informed consent

Exclusion criteria

.

  • Diabetes mellitus
  • Severe cardiovascular disease
  • Active malignant disease
  • Pregnancy or breast feeding
  • treatment with interfering drugs
  • Intake of grapefruit juice

Treatment and study plan

Solu-Cortef

Drug

administration by pump for minimum 2 weeks

Other names: hydrocortisone

Cortef

Drug

tablet treatment 2 ro 3 times per day for 14 days

Other names: hydrocortisone tablets

Primary outcomes

  1. Serum cortisol -24 hours curve

    Time frame: 24 hours

    admission to hospital for 24 hours

Secondary outcomes

  1. Salivary cortisol - 24 hours curve

    Time frame: 24 hours

    admission to the hospital for 25 hours

  2. 24 h urine cortisol and metabolites

    Time frame: 24 hours

    urine samples for 24 hours

  3. levels of corticotropic hormone

    Time frame: 24 hours

    blood samples

  4. 24 hours curve of tissue cortisol

    Time frame: 24 hours

    The tissue effect of glucocorticoid replacement - 24 hours curve of tissue cortisol (microdialysis)

  5. gene expression

    Time frame: 24 hours

    m RNA expression of genes

Sponsors and collaborators

Lead sponsor

Haukeland University Hospital

Other

Registry information

Important dates

Study start
2014
Primary completion
2016
Study completion
2017
First posted
Mar 26, 2014
Registry last updated
Jun 7, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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