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Effects of Steroid Replacement Therapy on Metabolic, Cardiovascular and Bone Outcomes in Adrenal Insufficiency

Conventional Glucocorticoids vs. Dual-release Hydrocortisone Effects on Metabolic, Cardiovascular, and Bone Outcomes in Treatment-naïve Patients With Adrenal Insufficiency: a 10-year Prospective Randomised Study

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06260462
Enrollment
88
Registered
2024-02-15
Start date
2012-01-01
Completion date
2023-12-30
Last updated
2024-02-15

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

Conditions

Adrenal Insufficiency

Brief summary

The current study is a randomized, open study aimed to compare the effects of conventional glucocorticoid replacement treatment and dual-release hydrocortisone on anthropometric, metabolic, cardiovascular and bone outcomes in treatment-naïve patients with primary adrenal insufficiency and secondary adrenal insufficiency in a 10 year-observation period.

Detailed description

Adrenal insufficiency (AI) can be caused by a disease involving the adrenal gland resulting in inadequate secretion of adrenal cortex hormones, primary adrenal insufficiency (PAI). Secondary adrenal insufficiency (SAI) results from a decreased level of adrenocorticotrophin hormone (ACTH) released from the pituitary gland. The mainstay of treatment of PAI and SAI is glucocorticoid (GC) replacement therapy. Conventional steroid replacement therapy includes cortisone acetate and hydrocortisone administered 2-3 times a day with the highest dose in the morning and the lowest dose in the afternoon. These dosing regimens have been designed to mimic the peak of cortisol secretion in the morning and avoid overdosing during the night hours, even though a higher risk of developing comorbidities has been shown, notably in patients treated with higher evening doses. In patients with AI on conventional steroid replacement therapy, mortality remains higher than in the general population, mainly due to non-physiological daily GC overexposure and to inadequate cortisol exposure during stress-related events and illness. Studies aiming to evaluate the long-term clinical outcomes of patients with AI on conventional steroid replacement therapy clearly showed increased comorbidities, mainly related to the dose used. By contrast, dual-release hydrocortisone (DR-HC) is characterized by once-daily administration with high release of hydrocortisone immediately after intake and a very low release in the evening and nocturnal hours. The switch from conventional GC therapy to DR-HC has been shown to be associated with improvement in BMI, hepatic, bone and glucometabolic parameters and QoL. However, long-term clinical outcomes of patients treated with DR-HC in patients naïve to steroid treatment are not known.

Interventions

DRUGdual-release hydrocortisone

Oral tablets 20-25-30-40 mg/day

DRUGConventional glucocortidois

Oral tablets 10-15-20-25-37,5-50-62,5 mg/day

Sponsors

University of Palermo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Adrenal insufficiency

Exclusion criteria

*

Design outcomes

Primary

MeasureTime frameDescription
Change of body weight0, 5 years, 10 yearsSingle outcome measurement of body weight (kg).

Secondary

MeasureTime frameDescription
Change of metabolic parameters0, 5 years and 10 yearsComposite outcome including evaluation of total cholesterol, HDL cholesterol, LDL cholesterol and triglycerides, HbA1c and fasting blood glucose
Change of insulin sensitivity parameters0, 5 years and 10 yearsthe Isi-Matsuda index
Change of cardiovascular parameters0, 5 years and 10 yearsMeasurement of interventricular septum at diastole (IVSd) and the thickness of the posterior wall (PWT) by high-resolution M-B-mode transthoracic echocardiography
Change of anthropometric parameters0, 5 years and 10 yearswaist circumference
Change of bone density0, 5 years and 10 yearsBone mineral density quantified by Dual X-Ray Absorptiometry (DEXA)
Change of vascular parameters0, 5 years and 10 yearsMeasurement carotid intima media thickness by high-resolution M-B-mode echography
Change of bone metabolic parameters0, 5 years and 10 yearsComposite outcome including calcium, phosphorus, Vitamin D, PTH, creatinine (all measured in mg/dL)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026