Sequential Therapies After Osteoanabolic Treatment
Recruiting now
Conditions studied: Osteoporosis, Postmenopausal
In brief
12-month prospective, open-label, multicenter, international, observational study evaluating sequential treatments after osteoanabolics
Key facts
- Study ID
- NCT06164795
- Run by
- 424 General Military Hospital
- People needed
- 150
- Starts
- 2023-11-25
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2026-07-22
Who can join
Age: 50 and older, up to 85. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Postmenopausal women treated with severe osteoporosis completing their course with romosozumab or teriparatide
You may not qualify if…
- a bone disease other than postmenopausal osteoporosis
- use of medications other than romosozumab or teriparatide affecting bone metabolism during the last 12 months before entering the study
- creatinine clearance <60 mL/min/1.73 m2
- liver failure
- any type of cancer
- uncontrolled endocrine diseases
- serum 25-hydroxy vitamin D (25-OHD) concentrations lower than 20 ng/mL (50 nmol/L)
- hypersensitivity to denosumab or zoledronate or teriparatide or romosozumab or any of the excipients
Where it is running
- 251 Airforce & VA General Hospital — Athens, Greece (enrolling)
- First Department of Propaedeutic and Internal Medicine, Medical School, National and Kapodistrian University of Athens — Athens, Greece (enrolling)
- , KAT General Hospital — Athens, Greece (enrolling)
- 424 General Military Hospital — Thessaloniki, Greece (enrolling)
- Fondazione IRCCS Cà Granda-Ospedale Maggiore Policlinico — Milan, Italy (enrolling)
- Campus Bio-Medico University — Roma, Italy (enrolling)
- Department of Medicine, Surgery and Neurosciences, University of Siena — Siena, Italy (enrolling)
- University-Hospital S. Maria della Misericordia — Udine, Italy (enrolling)
Full record on ClinicalTrials.gov
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