NL-OMON34558
Completed
Not Applicable
Identification of psychometric and biological markers to assess androgen and serotonergic sensitivity in relation to sexual functioning in women. - Androgen sensitivity in women.
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Female Sexual Dysfunction
- Sponsor
- Emotional Brain
- Enrollment
- 200
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility 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 \<\= 30 kg/m2;
- •6\. Dutch as first language;
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.
Outcomes
Primary Outcomes
Not specified
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