Vascular Function, Sarcopenia and Pain in Postmenopausal Osteoporosis
Recruiting · NCT05228262 · Interventional (participants receive a specific treatment) · Lead sponsor: University Hospital, Clermont-Ferrand
View the official record on ClinicalTrials.gov →Interventions studied
Cohort follow-up
What this trial is about
This study aims to follow a cohort of osteoporotic patients treated with anti-osteoporotic drugs and to evaluate the impact of these treatments on the osteoporosis-cardiovascular-sarcopenia triad and on pain.
Who can take part
Age range
50 Years and older
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Women aged 50 years or older with postmenopausal osteoporosis, whether fractured or not, requiring initiation of treatment with antiosteoporotic drugs (bisphosphonates, raloxifene, teriparatide, denosumab and others to come for this indication, including romosozumab), either orally or by injection, as part of their care and management.
- Able to give informed consent to participate in research.
- Affiliation to a Social Security system.
Exclusion criteria
- Patient with chronic renal failure, defined as glomerular filtration rate \< 30 mL.min-1 estimated by CKD-EPI.
- Patient with a medical and/or surgical history deemed by the investigator or his/her representative to be incompatible with the trial.
- Patient under legal protection or deprived of liberty.
- Refusal to participate.
Where it is running
1 location listed.
- CHU de Clermont-Ferrand - Clermont-Ferrand, France