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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
Marianne Andersen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Adrenal Insufficiency focused on measuring tertiary adrenal insufficiency

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
January 2, 2022
Last Updated
November 23, 2022
Sponsor
Marianne Andersen
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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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