How short steroid treatments change bone turnover markers in people with inflammatory joint disease
Official title: Dynamics in Bone Turnover Markers During and After Short-term Glucocorticoid Treatment in Patients With an Inflammatory Joint Disease - the BOOGIE Study
Run by Diakonhjemmet Hospital · NCT06395883 · Data updated 2026-11-12
This project will test whether short courses of glucocorticoids change blood bone-turnover tests in people with inflammatory joint disease who are not on osteoporosis therapy.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 25 Years to 90 Years |
| Sex | All |
| Enrollment | 160 (estimated) |
| Sponsor | Diakonhjemmet Hospital Academic / other |
| Locations | 2 sites (Drammen and 1 other locations) |
| Status | Recruiting |
| Started | January 1, 2025 |
| Main results expected | October 2027 |
| Study ends | December 2028 |
| Registry record updated | August 19, 2026 |
| Trial ID | NCT06395883 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with an inflammatory rheumatic joint disease who need short-term glucocorticoid treatment or parenteral glucocorticoid injection and are not on osteoporosis medication, without recent fractures or chronic steroid use, are ideal candidates.
✕Probably not a fit
People already diagnosed with osteoporosis or on osteoporosis treatment, those with chronic glucocorticoid use, recent fractures, active cancer, kidney failure, or women in the transitory phase are excluded and unlikely to benefit from this project.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study follows patients with inflammatory rheumatic joint disease who either start disease-modifying therapy with or without short-term glucocorticoids or receive a parenteral glucocorticoid injection while on stable DMARDs. Blood bone-turnover markers (BTMs) will be measured before, during, and after the short glucocorticoid exposure to document the size and timing of changes. Patients with prior osteoporosis, recent fractures, chronic steroid use, active cancer, or kidney failure are excluded to avoid confounding. The goal is to define how reliably BTMs reflect bone metabolism surrounding short steroid courses to guide clinical interpretation and management.
Why it matters
Potential benefit: If successful, the results could help clinicians interpret BTM blood tests around steroid use and improve osteoporosis care and fracture prevention.
How similar studies have gone: Previous research shows glucocorticoids substantially suppress BTMs (often by ~30%), but the timing and recovery after short steroid courses is not well defined.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * diagnosis of inflammatory rheumatic joint disease * indication of disease modifying treatment initiation with or without glucocorticoids OR * stable DMARD treatment with parenteral glucocorticoid injection Exclusion Criteria: * known osteoporosis or osteoporosis treatment * women during the transitory phase * oestrogen treatment * any fracture within the last year * chronic glucocorticoid treatment * glucocorticoid treatment within the last year prior to inclusion * active cancer * kidney failure
Where it's running
-
Vestre Viken HF, Drammen
Drammen, Norway Recruiting -
Diakonhjemmet hospital
Oslo, Norway Recruiting
Study contacts
- Study coordinator: Birgitte Nellemann Nellemann, MD PHD
- Email: birgittenellemann@gmail.com
- Phone: +4747957020
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.