Female Sexual Dysfunction
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Provision of written informed consent; 2. Female 21-70 years of age; 3. Healthy according to normal results of medical history 4. Subject must be heterosexually oriented; 5. BMI >= 18 and
Exclusion criteria
Exclusion criteria: 1. Subjects who have had hand surgery interfering with measurement of digit lengths; 2. Subjects with musculoskeletal conditions affecting the measurements of digit lengths; 3. Known conditions associated with abnormal prenatal androgen exposure, namely congenital adrenal hyperplasia and complete androgen insensitivity syndrome; 4. Positive drug test and/or positive alcohol test; 5. Subjects with dyslexia; 6. Subjects who are color-blind; 7. Positive urine pregnancy test; 8. Use of oral contraception containing anti-androgens (e.g. Diane 35; Minerva); 9. Use of oral contraception containing 50 µg estrogen or more; 10. Homosexual orientation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. [CAG]n 2. Calculated second to fourth digit ratio 3. Pre-attentional bias for erotic stimuli (Stroop task) 4. Blood serum free testosterone levels | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Blood serum levels ADT-G, 3a-diol-G, DHEA and DHEA(s) 2. Genotype SERT and 5HT1a receptor 3. Questionnaires: SAQ, SSEQ and SMQ | — |
Countries
Netherlands