Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact
Recruiting Observational

Prevalence of Adrenal Insufficiency and Associated Factors in Rheumatoid Arthritis Patients Using Low-dose Corticosteroids.

NCT07866326 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-07-31
Last updated
2026-10-08

Condition(s) studied

Reumatoid ArthritisCorticosteroids Adverse ReactionAdrenal Insufficiency

Investigational drug(s) / intervention(s)

ACTH stimulation testCortisol

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

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Participants diagnosed with rheumatoid arthritis according to the 2010 ACR/EULAR criteria. * Participants who have been undergoing corticosteroid treatment for at least 3 weeks. * Participants in remission or with low disease activity (DAS28-CRP ≤3.2). Exclusion Criteria: * Patients with primary adrenal insufficiency. * Participants who have received pulse steroid therapy within the last 6 months. * Pregnancy and lactation. * Hypopituitarism * Uncontrolled diabetes mellitus * Comorbidities; ≥NYHA Class 3 heart failure, Stage 3 chronic kidney failure, ≥Child-Pugh Class B liver cirrhosis

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)

FacilityCityRegionStatus
SBU Bursa Yüksek İhtisas EAH Bursa Yıldırım Recruiting
Official registry record

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