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Inhalation/Nasal Corticosteroids and Prevalence of Hypothalamic-pituitary-adrenal (HPA) Axis Suppression in Human Immunodeficiency Virus (HIV)-Patients (Incorporate)

Primary Purpose

Adrenal Insufficiency

Status
Unknown status
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
ACTH stimulation test
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Adrenal Insufficiency focused on measuring adrenal insufficiency, adverse drug reaction, corticosteroid

Eligibility Criteria

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

Inclusion Criteria:

  • Receive a treatment for HIV-infection
  • > 18 years old
  • Current usage of inhalation or nasal corticosteroids, for at least two weeks
  • Willing to give informed consent

Exclusion Criteria:

  • adrenal insufficiency
  • Concurrent use of topical corticosteroids, usage of oral corticosteroids in the last three months. Intramuscular or intra-articular corticosteroid injections in the last year.
  • Contra-indications for tetracosactide: allergy for tetracosactide, Cushings's syndrome, refractory heart failure, peptic ulcer, acute psychosis, adrenogenital syndrome
  • If the patient ever had an ACTH-stimulation test before
  • Pregnant female or breast-feeding female.
  • Use of oral contraceptives, since these can heighten the cortisol-binding globulin
  • Exclusion criterion for the cortisol measurements in hair: baldness

Sites / Locations

  • Onze lieve vrouw GasthuisRecruiting
  • Radboud UMCRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

ACTH stimulation test

Arm Description

this is a single arm study. An ACTH-stimulation test will be done

Outcomes

Primary Outcome Measures

the percentage of participants with a morning serum cortisol below 80 nmol/L in morning or below 550 nmol/L after Adrenocorticotropic (ACTH) stimulation test
these are the persons with hypothalamic-pituitary-adrenal (HPA) -axis suppression

Secondary Outcome Measures

Difference in percentage of HPA-axis suppression in participants who use a Cytochrome P450 3A4 (CYP3a4) inhibitor (ritonavir or cobicistat) versus percentage of HPA-axis suppression in participants who don't use a booster
HPA-axis suppression is described in outcome 1. If the investigators have enough data the following will also be analysed: duration of usage of inhalation/nasal corticosteroids and use of systemical corticosteroid before (never versus ever used).
Percentage of HPA-axis suppression stratified by type of corticosteroid
HPA-axis suppression is described in outcome 1. If the investigators have enough data the following will also be analysed: duration of usage of inhalation/nasal corticosteroids and use of systemical corticosteroid before (never versus ever used).
Difference in percentage of HPA-axis suppression in persons who use a high dose of corticosteroids versus a low dose of corticosteroids
Cortisol measurements in hair to diagnose HPA-axis suppression, in comparison with serum cortisol or an ACTH stimulation test
hair cortisol measurements are given in pg/mg hair.

Full Information

First Posted
June 2, 2015
Last Updated
October 12, 2016
Sponsor
Radboud University Medical Center
Collaborators
AIDS Fonds, OLVG
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1. Study Identification

Unique Protocol Identification Number
NCT02501486
Brief Title
Inhalation/Nasal Corticosteroids and Prevalence of Hypothalamic-pituitary-adrenal (HPA) Axis Suppression in Human Immunodeficiency Virus (HIV)-Patients
Acronym
Incorporate
Official Title
Inhalation or Nasal Corticosteroids and Prevalence of Hypothalamic-pituitary-adrenal Axis Suppression in HIV-infected Patients
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Unknown status
Study Start Date
July 2015 (undefined)
Primary Completion Date
January 2017 (Anticipated)
Study Completion Date
February 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center
Collaborators
AIDS Fonds, OLVG

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Rationale: Case reports describe suppression of the hypothalamic-pituitary-adrenal (HPA) axis caused by local corticosteroids, most often with inhalation corticosteroids. The exact prevalence is not known. Early recognition is important, because suppression of the HPA-axis can lead to significant morbidity and mortality. Suppression of the HPA axis might occur more often when a Cytochrome P450 3A4 (CYP3A4) inhibitor, e.g. ritonavir, is used next to the local corticosteroid, a combination often used by human immunodeficiency virus (HIV)-patients. Cortisol can be determined in hair. This non-invasive analysis could help in diagnosis of suppressed HPA-axis. Research questions: Primary objective: How often do inhalation or nasal corticosteroids lead to suppression of the HPA- axis in HIV-treated patients? Secondary objectives: Are other variables associated with the HPA-axis suppression? Are cortisol measurements in hair as reliable as serum cortisol or an Adrenocorticotropic hormone (ACTH) stimulation test to diagnose suppression of the HPA axis? Study design: cross-sectional explorative study Study population: adults treated for HIV and using an inhalation or nasal corticosteroid. Intervention: an ACTH stimulation test, cortisol measurements in blood and hair. Main study parameters/endpoints: Proportions of persons with a low morning plasma cortisol or low cortisol after an ACTH stimulation test. Correlation between cortisol in plasma and hair cortisol. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Each person will be screened with a history and a short physical examination. A venous cannula will be inserted for obtaining blood for the plasma cortisol and for the ACTH stimulation test. An ACTH stimulation test has no major complications. A piece of hair is cut for cortisol hair analysis. The risks and burden are minimal, while the future benefits could be great since suppression of the endogenous HPA- axis can be associated with morbidities like hypertension or osteoporosis and can even lead to an adrenal crisis when the local corticosteroid is stopped.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adrenal Insufficiency
Keywords
adrenal insufficiency, adverse drug reaction, corticosteroid

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ACTH stimulation test
Arm Type
Other
Arm Description
this is a single arm study. An ACTH-stimulation test will be done
Intervention Type
Other
Intervention Name(s)
ACTH stimulation test
Intervention Description
An ACTH stimulation test will be done
Primary Outcome Measure Information:
Title
the percentage of participants with a morning serum cortisol below 80 nmol/L in morning or below 550 nmol/L after Adrenocorticotropic (ACTH) stimulation test
Description
these are the persons with hypothalamic-pituitary-adrenal (HPA) -axis suppression
Time Frame
baseline
Secondary Outcome Measure Information:
Title
Difference in percentage of HPA-axis suppression in participants who use a Cytochrome P450 3A4 (CYP3a4) inhibitor (ritonavir or cobicistat) versus percentage of HPA-axis suppression in participants who don't use a booster
Description
HPA-axis suppression is described in outcome 1. If the investigators have enough data the following will also be analysed: duration of usage of inhalation/nasal corticosteroids and use of systemical corticosteroid before (never versus ever used).
Time Frame
baseline
Title
Percentage of HPA-axis suppression stratified by type of corticosteroid
Description
HPA-axis suppression is described in outcome 1. If the investigators have enough data the following will also be analysed: duration of usage of inhalation/nasal corticosteroids and use of systemical corticosteroid before (never versus ever used).
Time Frame
baseline
Title
Difference in percentage of HPA-axis suppression in persons who use a high dose of corticosteroids versus a low dose of corticosteroids
Time Frame
baseline
Title
Cortisol measurements in hair to diagnose HPA-axis suppression, in comparison with serum cortisol or an ACTH stimulation test
Description
hair cortisol measurements are given in pg/mg hair.
Time Frame
baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Receive a treatment for HIV-infection > 18 years old Current usage of inhalation or nasal corticosteroids, for at least two weeks Willing to give informed consent Exclusion Criteria: adrenal insufficiency Concurrent use of topical corticosteroids, usage of oral corticosteroids in the last three months. Intramuscular or intra-articular corticosteroid injections in the last year. Contra-indications for tetracosactide: allergy for tetracosactide, Cushings's syndrome, refractory heart failure, peptic ulcer, acute psychosis, adrenogenital syndrome If the patient ever had an ACTH-stimulation test before Pregnant female or breast-feeding female. Use of oral contraceptives, since these can heighten the cortisol-binding globulin Exclusion criterion for the cortisol measurements in hair: baldness
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
F Besemer
Phone
0031243614599
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Burger, Prof
Organizational Affiliation
Radboud UMC Pharmacy
Official's Role
Principal Investigator
Facility Information:
Facility Name
Onze lieve vrouw Gasthuis
City
Amsterdam
Country
Netherlands
Individual Site Status
Recruiting
Facility Name
Radboud UMC
City
Nijmegen
Country
Netherlands
Individual Site Status
Recruiting

12. IPD Sharing Statement

Citations:
PubMed Identifier
32140912
Citation
Besemer F, Kramers C, Brinkman K, Hermus ARMM, van Herwaarden AE, Burger DM. Hypothalamic-pituitary-adrenal axis suppression by inhaled or nasal corticosteroids in HIV-infected patients. Int J Clin Pharm. 2020 Apr;42(2):347-350. doi: 10.1007/s11096-020-00995-5. Epub 2020 Mar 5.
Results Reference
derived

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Inhalation/Nasal Corticosteroids and Prevalence of Hypothalamic-pituitary-adrenal (HPA) Axis Suppression in Human Immunodeficiency Virus (HIV)-Patients

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