Hydrocortisone and Placebo in Patients With Partial Adrenal Insufficiency After Cessation of Glucocorticoid Treatment (REPLACE)
Primary Purpose
Adrenal Insufficiency
Status
Recruiting
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Hydrocortisone
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Adrenal Insufficiency focused on measuring tertiary adrenal insufficiency
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 50 years
- A diagnosis of PMR or GCA in GC free remission for >2 week and <12 weeks after treatment with prednisolone (any dosage) for ≥12 weeks
Exclusion Criteria:
- Known primary or secondary adrenal insufficiency
- Known Cushing´s syndrome
- Heart failure (New York Heart Association class IV)
- Kidney failure with an estimated glomerular filtration rate <30 mL/min
- Liver cirrhosis
- Active cancer
- Known severe immune deficiency
- A history of psychiatric disease requiring treatment by a psychiatric department (for affective disorders only if within the last year before study entry)
- Alcohol consumption >21 units per week
- Planned major surgery during the study period at study entry
Sites / Locations
- OdenseUHRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Placebo
Hydrocortisone
Arm Description
Placebo tablets
hydrocortisone tablets
Outcomes
Primary Outcome Measures
Adrenal insufficiency symptoms
measured by questionaire: AddiQoL-30
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05193396
Brief Title
Hydrocortisone and Placebo in Patients With Partial Adrenal Insufficiency After Cessation of Glucocorticoid Treatment
Acronym
REPLACE
Official Title
A Randomised, Placebo Controlled to Compare the Effect of Hydrocortisone and Placebo in Patients With Partial Adrenal Insufficiency After Cessation of Glucocorticoid Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2022 (Actual)
Primary Completion Date
February 2024 (Anticipated)
Study Completion Date
February 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Marianne Andersen
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Cortisol, a glucocorticoid (GC) hormone secreted from the adrenal glands, is essential for survival.Cortisol also possesses anti-inflammatory actions and GC formulations (prednisolone) are used to treat many inflammatory diseases and conditions. Indeed, three percent of the Danish population(≈ 180.000 individuals) redeems at least one prescription of synthetic GC per year and at least 20,000 patients annually discontinue GC treatment. Pharmacological GC therapy suppresses endogenous cortisol production and thereby induce relative adrenal insufficiency (GIA). The risk of GIA as determined by the adrenal corticotrophic hormone (ACTH) stimulation test is ≈ 25 %,but testing after GC treatment is not routinely performed. In addition, the ACTH stimulation testwas developed for the diagnosis of complete primary adrenal insufficiency, wherefore the clinical value of the ACTH stimulation test in the context of GIA is unknown. When diagnosed, GIA is treated with hydrocortisone (equivalent to cortisol). Excess GC exposure is associated with very serious adverse effects which may also apply to hydrocortisone treatment in patients with GIA. Moreover, hydrocortisone treatment may postpone normalization of adrenal function. On the other hand, GIA patients may develop symptomatic adrenal insufficiency that justifies hydrocortisone treatment. Despite these dilemmas, no evidence-based data exist regarding the proper management of GIA patients. The study is a multi-centre, randomised, double-blinded, placebo controlled 1-year study to compare the effect of hydrocortisone and placebo in patients with Giant Cell Arterititis or Polymyalgia Rheumatica (PMR) with partial adrenal insufficiency after cessation of glucocorticoid treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adrenal Insufficiency
Keywords
tertiary adrenal insufficiency
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
150 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo tablets
Arm Title
Hydrocortisone
Arm Type
Active Comparator
Arm Description
hydrocortisone tablets
Intervention Type
Drug
Intervention Name(s)
Hydrocortisone
Intervention Description
hydrocortisone
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
placebo tablets
Primary Outcome Measure Information:
Title
Adrenal insufficiency symptoms
Description
measured by questionaire: AddiQoL-30
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥ 50 years
A diagnosis of PMR or GCA in GC free remission for >2 week and <12 weeks after treatment with prednisolone (any dosage) for ≥12 weeks
Exclusion Criteria:
Known primary or secondary adrenal insufficiency
Known Cushing´s syndrome
Heart failure (New York Heart Association class IV)
Kidney failure with an estimated glomerular filtration rate <30 mL/min
Liver cirrhosis
Active cancer
Known severe immune deficiency
A history of psychiatric disease requiring treatment by a psychiatric department (for affective disorders only if within the last year before study entry)
Alcohol consumption >21 units per week
Planned major surgery during the study period at study entry
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marianne S Andersen
Phone
+4565411807
Email
marianne.andersen1@rsyd.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marianne S Andersen
Organizational Affiliation
Odense University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
OdenseUH
City
Odense
ZIP/Postal Code
5230
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marianne Andersen, DMSci
12. IPD Sharing Statement
Plan to Share IPD
Undecided
IPD Sharing Plan Description
undecided
Learn more about this trial
Hydrocortisone and Placebo in Patients With Partial Adrenal Insufficiency After Cessation of Glucocorticoid Treatment
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