gezonde deelnemers healthy controls
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Female - Age > 18 years - For postmenopausal women: at least 1 year after menopause - For premenopausal women: a regular menstruation - Signed written informed consent
Exclusion criteria
Exclusion criteria: - Use of estrogen receptor ligands - History of ER-positive malignancies or breast cancer - Use of any contraceptive drug (pill, injections or implanted) - For postmenopausal women: (history of) estrogen replacement therapy - Pregnancy - History of removal of the ovaries and/or the uterus - Current systemic and or major metabolic diseases - Somatic, organic or neurological disorders - Recent participation in a scientific research study (
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameters are the binding potential and distribution volume of [18F]FES in the human brain, derived from kinetic modelling using an arterial input function, reference tissue modelling and an image derived input function. | — |
Secondary
| Measure | Time frame |
|---|---|
| A secondary study parameter is the level of estradiol in serum. | — |
Countries
Netherlands