Prevalence of Adrenal Insufficiency and Associated Factors in Rheumatoid Arthritis Patients Using Low-dose Corticosteroids.
Condition(s) studied
Investigational drug(s) / intervention(s)
ACTH stimulation test: ACTH stimulation test with 250 micrograms tetracosactide acetate if plasma cortisole is below 10 mcg/dl
Cortisol: morning fasting plasma cortisol
Study summary
This study aims to investigate the prevalence of adrenal insufficiency in rheumatoid arthritis (RA) patients receiving low-dose corticosteroid therapy and to identify the factors influencing adrenal insufficiency. To this end, the researchers plan to conduct a study comparing the prevalence of adrenal insufficiency and associated factors among RA patients-who are currently receiving low-dose corticosteroid therapy during outpatient follow-up and have consented to participate-by categorizing them into three groups based on the duration of treatment: short (3 weeks-3 months), medium (3-12 months), and long (\>12 months).
Eligibility
Primary outcome measure(s)
- prevalence of adrenal insufficiency — through study completion, an average of 1 year
The assessment of adrenal insufficiency is conducted in two stages: the morning cortisol level is measured in the first stage, and the ACTH stimulation test is administered to the relevant participants in the second stage. - DAS-28 — through study completion, an average of 1 year
Disease activity score for rheumatoid arthritis - HAQ — through study completion, an average of 1 year
Health Assessment Questionnaires - RAPİD-3 — through study completion, an average of 1 year
Routine Assessment of Patient Index Data 3 - PASI — through study completion, an average of 1 year
Psoriasis Area Severity Index
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| SBU Bursa Yüksek İhtisas EAH | Bursa | Yıldırım | Recruiting |
More Bursa Yuksek Ihtisas Training and Research Hospital trials in Turkey
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07866326 on ClinicalTrials.gov ↗ ← All trials in Turkey