Actively Recruiting
Sequential Therapies After Osteoanabolic Treatment
Led by 424 General Military Hospital · Updated on 2025-04-27
150
Participants Needed
8
Research Sites
179 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
12-month prospective, open-label, multicenter, international, observational study evaluating sequential treatments after osteoanabolics
CONDITIONS
Official Title
Sequential Therapies After Osteoanabolic Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Postmenopausal women treated for severe osteoporosis who have completed romosozumab or teriparatide treatment
You will not qualify if you...
- Presence of bone diseases other than postmenopausal osteoporosis
- Use of medications affecting bone metabolism other than romosozumab or teriparatide within 12 months prior to study entry
- Creatinine clearance less than 60 mL/min/1.73 m2
- Liver failure
- Any type of cancer
- Uncontrolled endocrine diseases
- Serum 25-hydroxy vitamin D levels below 20 ng/mL (50 nmol/L)
- Hypersensitivity to denosumab, zoledronate, teriparatide, romosozumab, or any excipients
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 8 locations
1
251 Airforce & VA General Hospital
Athens, Greece, 11525
Actively Recruiting
2
First Department of Propaedeutic and Internal Medicine, Medical School, National and Kapodistrian University of Athens
Athens, Greece, 11527
Actively Recruiting
3
, KAT General Hospital
Athens, Greece, 14561
Actively Recruiting
4
424 General Military Hospital
Thessaloniki, Greece, 56429
Actively Recruiting
5
Fondazione IRCCS Cà Granda-Ospedale Maggiore Policlinico
Milan, Italy
Actively Recruiting
6
Campus Bio-Medico University
Roma, Italy, 00128
Actively Recruiting
7
Department of Medicine, Surgery and Neurosciences, University of Siena
Siena, Italy, 53100
Actively Recruiting
8
University-Hospital S. Maria della Misericordia
Udine, Italy
Actively Recruiting
Research Team
A
Athanasios D Anastasilakis, PhD
CONTACT
J
John Carey, Prof
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
6
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