ClinicalTrials.gg
Status unknownNCT01771328CAHUpdated Dec 21, 2016

Continuous Subcutaneous Hydrocortisone Infusion in Congenital Adrenal Hyperplasia

A Phase 2 interventional study of Hydrocortisone and Cortisone acetate in Adrenal Hyperplasia, Congenital, sponsored by Haukeland University Hospital. Status unknown at 1 site in Norway. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2016-12-21.

Sponsored by Haukeland University Hospital · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2016), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 17 studies testing hydrocortisone in Adrenal Hyperplasia, Congenital — 1 open to participants now, 1 under way, none of them phase 3. Hydrocortisone · Adrenal Hyperplasia, Congenital.

Planned enrollment
10th of 17
20 · median 28
Started
2013
with 1 other
Phase 2
3 of 17
none open now
Registered
5th of 17
by date
Lead sponsor
2 of 17
Haukeland University Hospital

Among the 17 studies testing hydrocortisone in Adrenal Hyperplasia, Congenital, this one is the 10th largest by planned enrollment, is one of 2 that started in 2013, is one of 3 in phase 2, and was the 5th registered.

By phase

17 studies; the count open now beside each. This study's row is marked.

Phase 36 · 0 open
Phase 13 · 0 open
Phase 2this study3 · 0 open
Phase 1/22 · 0 open
Phase 42 · 1 open
No phase1 · 0 open

By the year they started

First in 1995; this study’s year is marked. 2 started in 2013.

Size and results

Median enrollment 28 across the 17 interventional studies. Of the 13 that completed or were terminated, 8 (62%) have results posted.

Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 17 studies testing hydrocortisone in Adrenal Hyperplasia, Congenital, or all of them as a file.
02

Study summary

The conventional glucocorticoid replacement therapy in congenital adrenal hyperplasia (CAH) renders the cortisol levels unphysiological, which may cause symptoms and long-term complications. Glucocorticoid replacement is technically feasible by continuous subcutaneous hydrocortisone infusion (CSHI), and can mimic the normal diurnal cortisol rhythm. This method was recently applied to treat a patient through a critical phase of puberty. This is a clinical trial aiming to evaluate CSHI treatment in patients with CAH. The main objective is to determine the effects of CSHI on metabolic parameters (androstenedione and 17-hydroxyprogesterone profiles, and testosterone,adrenocorticotropic hormone(ACTH), cortisol, and bone markers), and to determine the required glucocorticoid doses. Secondary objectives are to determine effects on clinical status, body weight, blood pressure and other metabolic parameters, as well as on subjective health status (AddiQoL, SF36).

Read the detailed description

CAH patients are treated with glucocorticoids and mineralocorticoids. Ideally, the glucocorticoid doses should be sufficient to suppress the elevated ACTH secretion, and hence attenuate the increase in androgen levels. Because of this, CAH patients use higher steroid doses than patients with autoimmune adrenal insufficiency (Addison's disease) and therefore are in higher risk of developing glucocorticoid side effects. The natural glucocorticoids, hydrocortisone (cortisol) or cortisone acetate, are preferred during childhood because of the growth suppressive effects of the longer acting synthetic glucocorticoids, prednisolone and dexamethasone. There is no consensus as to which type of glucocorticoid and which doses should be used for adult CAH patients. Glucocorticoids display a typical diurnal variation, which the current therapy does not restore, leading to both to over- or undertreatment. Some CAH patients experience symptoms that may be due to unphysiological glucocorticoid replacement therapy.

For selected CAH patients with poor response to conventional replacement therapy, or with problematic side effects such as impaired growth, weight gain, metabolic syndrome, and osteoporosis, continuous subcutaneous hydrocortisone infusion (CSHI) might become a treatment option. CSHI treatment would also be facilitated by the use of the small disposable pumps now developed for insulin treatment.

CSHI: Pharmacodynamics, Pharmacokinetics, and safety Hydrocortisone is identical to cortisol; the pharmacodynamics does not depend on mode of delivery. A hydrocortisone solution can be safely applied for three days in the insulin pump without major day-to-day variation. A daily dose of 10 mg/m2 body surface area/day restores normal levels of saliva cortisol in most patients. Thus, it is possible to mimic the physiological diurnal cortisol variation seen in healthy subjects.

The study will compare two glucocorticoid replacement modalities in randomised order within each patient. Prior to Baseline there will be a period of dose adjustment for pump treatment. Patients will be educated in groups, and dose adjustments will be co-ordinated with regular visits at the outpatient clinic/telephone consultation combined with laboratory analyses.

The patients will be assigned a participation number and randomised to any of two treatment sequences (A-B or B-A). Should the need for an extra glucocorticoid dose occur (intercurrent illness) during the study, the patients should administer their previous glucocorticoid replacement for safety reasons. Extra doses should be recorded in the patient diary. Treatment A is current treatment, i.e. glucocorticoid and mineralocorticoid replacement according to best clinical judgement. Treatment B is CSHI with the initial standard dose of 10mg/m2/24hrs. Body surface area will be calculated according to the nomogram from the formula of Du Bois and Du Bois.

After 7 days after initiating pump therapy the patient should be reassessed with blood dots (17-hydroxyprogesterone) and saliva cortisol and saliva 17-hydroxyprogesterone measurements in the morning (0800-0900) and in the evening (2300-2400). Based on results of this testing the dose will be changed at the discretion of the investigator. The further new testing should be done within 7-10 days.

When the final dose is established a 24h urine measurement, blood test in the morning (17-hydroxyprogesterone and cortisol) and a salivary sample full profile (full profile Hrs. 0800, 0930, 1100, 1230, 1700, 2100, 2400, 0300), will be done before entering the study. The dose adjustment period will be unlimited but will take minimally 4 weeks (aiming to obtain normal range levels of morning serum cortisol (160- 620 nmol/l), and 3-4 times increase in morning serum 17-hydroxyprogesterone (0,3-8,6 nmol/l for females, 0,9-6,6 nmo/l for males), and midnight (24:00) saliva cortisol (\<2,8 nmol/l) and a circadian pattern as indicated in figure 1.

Afterwards it will 4 weeks wash out period before starting, wash out period between treatments modalities will take 2 months.

03

Conditions studied

  • Adrenal Hyperplasia, Congenital

Keywords

  • Adrenal Hyperplasia, Congenital
04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • verified salt-wasting CAH and simple virilizing CAH, on single prednisone, or hydrocortisone therapy.
  • In case of concomitant endocrine/ diseases these should be on stable treatment during the study period.

Exclusion criteria

Exclusion Criteria:

  • Patients with diabetes mellitus on insulin pump treatment will not be included in this study
  • cardiovascular disease, active malignant disease and pregnancy, and pharmacological treatment with or drugs that interfere with cortisol metabolism (antiepileptics, rifampicin, St. Johns wart).
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Active comparator
    hydrocortisone

    Treatment B ( Solu-Cortef) the initial standard dose of 10mg/m2/24hrs. Hydrocortisone infusate will be given as Solu-Cortef Act-o-Vial 50mg/ml, produced by Pfizer. Treatment will take 4 months.

    Drug: Hydrocortisone

  • Active comparator
    cortisone acetate

    Treatment A (Cortisone tbl.) is current treatment, i.e. glucocorticoid and mineralocorticoid replacement according to best clinical judgement. This treatment period will take 6 months.

    Drug: Cortisone acetate

Interventions

  • Initial standard dose of 10mg/m2/24hrs administered by pump during the treatment period, it will take 4 months. Body surface area will be calculated according to the nomogram from the formula of Du Bois and Du Bois.

    Also known as: Solu-Cortef

  • Patients will take this tables two times during day according to best clinical practice of therapy of congenital adrenal hyperplasia. Usually Cortisone 25 mg 1 tbl. in the morning and Cortisone 25 1/4 tbl. in the evening. This period will take 6 months.

    Also known as: Cortisone

06

What researchers measure

Primary outcomes

  1. Androgen levels

    Androgen levels as parameters of adequate suppression of androgen production

    Time frame: 3 months

Secondary outcomes

  1. Steroid metabolism

    levels of ACTH

    Time frame: 4 months

  2. bone metabolism

    Time frame: 3 months

  3. fasting glucose

    Time frame: 4 months

  4. body mass index

    Time frame: 3 months

  5. Dual-energy X-ray absorptiometry (DXA)

    body composition, bone mineral density

    Time frame: 6 months

  6. Subjective health status

    questionnaire

    Time frame: 3 months

  7. waist circumference

    cm

    Time frame: 3 month

  8. hip circumference

    cm

    Time frame: 3 months

  9. blood pressure

    Time frame: 3 months

  10. fasting insulin

    Time frame: 3-4 months

  11. glycated haemoglobin (Hb1AC)

    Time frame: 4 months

  12. lipid levels

    Time frame: 4 months

  13. c-reactive protein

    Time frame: 4 months

  14. Steroid metabolism

    cortisol levels

    Time frame: 4 months

07

Study locations

1 of 1 sites recruiting
  • Haukeland Universitetssykehus, Department of Medicine
    Bergen, 5021, Norway
    Recruiting
    • Kristian Løvås, MD, PhD · Contactkral@helse-bergen.no · +4755977996
    • Katerina Simunkova, MD, PhD · Contactkaterina.simunkova@med.uib.no · +4755974603
    • Kristian Løvås, MD, PhD · Principal investigator
    • Marianne Øksnes, MD · Sub investigator
    • Ingrid Nermoen, MD · Sub investigator
    • Paal Methlie, MD · Sub investigator
    • Eystein S Husebye, prof., MD · Sub investigator
    • Katerina Simunkova, MD, PhD · Principal investigator
08

References and documents

Related links

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 21, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01771328
Responsible party
Sponsor
First posted
Jan 18, 2013
Start date
Feb 2013
Primary completion
Jan 2017 (estimated)
Completion
Jan 2017 (estimated)
Last update
Dec 21, 2016

Study contacts

Kristian Løvås, MD, PhD
Contact
kral@helse-bergen.no
+47 55977996
Katerina Simunkova, MD, PhD
Contact
katerina.simunkova@med.uib.no
+47 55974603
Kristian Løvås, MD, PhD
principal investigator · Haukeland University Hospital, Department of Medicine

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2016. You cannot join it, but the record below documents what was studied.

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Studies of the drugs tested here: Hydrocortisone · Cortisone

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