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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00476489
Other study ID # 02307EMC
Secondary ID
Status Recruiting
Phase N/A
First received May 21, 2007
Last updated May 21, 2007
Start date May 2007

Study information

Verified date May 2007
Source HaEmek Medical Center, Israel
Contact Avraham Ishay, MD
Phone 972-4-6495556
Email ishay_av@clalit.org.il
Is FDA regulated No
Health authority Israel: Ethics Commission
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine if topical steroids treatment for different skin diseases suppress the adrenal cortisol production.


Description:

Adrenocortical suppression is a potential complication of systemic corticosteroid treatement but also of non systemic therapy like topical therapy.

The normalcy of hypothalamic-pituitary-adrenal axis ( HPA axis) of patients with chronic skin diseases like atopic dermatitis, pemphigus or psoriasis which are treated with topical steroids, will be assessed with the low dose (1mcg) adrenocortocotropin ( ACTH) stimulation test. During this test serum cortisol levels are measured before, 30 and 60 mn after intravenous administration of 1mcg of ACTH (synacthen).The results will be compared with age and sex matched subjects with normal HPA axis as assessed by low dose ACTH stimulation test.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- patients receiving daily topical steroids for at least two weeks on 10% or more of body surface.

Exclusion Criteria:

- patients treated with any form of corticosteroids except topical steroids.

- patients with known pituitary disease

- pregnant patients

Study Design

Observational Model: Case Control, Primary Purpose: Screening, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Haemek Medical Center Afula

Sponsors (1)

Lead Sponsor Collaborator
HaEmek Medical Center, Israel

Country where clinical trial is conducted

Israel,