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Validation of [18F]FES for imaging of brain estrogen receptors

Validation of [18F]FES for imaging of brain estrogen receptors - [18F]FES for imaging of brain ER

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37068
Enrollment
12
Registered
2012-08-09
Start date
2013-01-01
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

gezonde deelnemers healthy controls

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

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

MeasureTime 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

MeasureTime frame
A secondary study parameter is the level of estradiol in serum.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)