osteoporosis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: female sex regular menstrual cycle and age 18 to 50 years OR 1-5 years postmenopausal
Exclusion criteria
Exclusion criteria: contraindications to MRI scanning use of bone-modifying or adipose tissue-modifying drugs use of hormonal contraception bone/adipose tissue/bone marrow diseases contraindications to estrogen treatment (history of hormone-sensitive cancer, VTE, unexplained vaginal bleeding, endometrial hyperplasia, endometriosis, arterial thrombo-embolic diseases, acute hepatic disease or liver enzyme disorders, porfyria or known hypersensitivity to components of zumenon)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameters are the dynamic changes in bone marrow adiposity as assessed by QCSI measurements and the correlation of these changes to changes in hormones involved in the menstrual cycle (follicle stimulating hormone, luteinizing hormone, progesterone and estradiol). | — |
Countries
Netherlands