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NCT06718985
Impact of Bone Mineral Density on Fracture Risk Assessment in RA
trial testing No intervention in Rheumatoid Arthritis in 60 participants. Completed in 4 April 2023.
4 April 2023
Quick facts
| Lead sponsor | Istanbul Physical Medicine Rehabilitation Training and Research Hospital |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 60 |
| Start date | 4 December 2022 |
| Primary completion | 4 April 2023 |
| Estimated completion | 4 April 2023 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- No intervention
Conditions studied
- Rheumatoid Arthritis — all drugs for Rheumatoid Arthritis →
Sponsor
Istanbul Physical Medicine Rehabilitation Training and Research Hospital
Who can join
Adults 40 to 90, any sex, with Rheumatoid Arthritis. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study investigates whether incorporating bone mineral density (BMD) into FRAX calculations changes fracture risk assessment and influences treatment decisions in rheumatoid arthritis (RA) patients. Analyzing 60 RA patients, FRAX scores for 10-year major osteoporotic and hip fractures were calculated with and without BMD. While no significant differences were found between the two methods, discrepancies in treatment recommendations were identified, particularly for hip fractures. The findings emphasize the importance of combining BMD and FRAX for a more comprehensive fracture risk assessment and informed treatment decision-making in RA patients.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06718985
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Istanbul Physical Medicine Rehabilitation Training and Research Hospital trials
Trials by the same sponsor.
- NCT07435935 — Bone Myoregulation Reflex and Postural Control in Vitamin D Deficiency · not yet recruiting
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- NCT07408570 — FREQUENCY-DEPENDENT SOLEUS REFLEX MODULATION DURING WHOLE-BODY VIBRATION · NA · enrolling by invitation
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06718985 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Istanbul Physical Medicine Rehabilitation Training and Research Hospital
- Last refreshed: 5 December 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06718985.
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