osteoporosis
Conditions
Interventions
The participants will be randomized to receive hormonal replacement therapy
(HRT) (zumenon 1dd 2 mg), HRT and beta-agonist (terbutaline 1dd 5 mg),
beta-antagonist (propranolol SR 1dd 80 mg) or no tr
Sponsors
Academisch Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: female sex last menstrual cycle 12-60 months ago
Exclusion criteria
Exclusion criteria: Contraindications to HRT, beta-agonist or beta-antagonist treatment, such as cardiovascular disease, astma, COPD, renal or hepatic insufficiency Any medication or disease influencing bone turnover Prior VTE or breast cancer Current osteoporosis defined by a DXA Z-score >-2.5
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameter is the difference in change of serum concentrations of bone turnover markers (procollagen type I N propeptide (P1NP) and C-terminal crosslinking telopeptides of collagen type I (CTX)) compared in the treatment and control groups(4). | — |
Secondary
| Measure | Time frame |
|---|---|
| A secondary parameter is the change in number of circulating stem cells and osteogenic cells(7). | — |
Countries
Netherlands
Outcome results
None listed