A study to investigate the efficacy of sublingual testosterone solution on physiological and subjective arousal in healthy, sexually dysfunctional premenopausal women.
Recruiting
- Conditions
- Female sexual dysfunction (FSD),Female Sexual Arousal Disorder, Hypoactive sexual desire disorder, sublingual testosterone
- Registration Number
- NL-OMON23272
- Lead Sponsor
- Emotional brain BV
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 16
Inclusion Criteria
For inclusion in the study, the subjects of the study group healthy women with Female Sexual Dysfunction must fulfill the following criteria:
1. Female 21-40 years of age with Hypoactive Sexual Desire Disorder (comorbidity with other sexual dysfunctions e.g Female Sexual Arousal Disorder (FSAD) is allowed). The diagnosis will be made by an experienced psychologist/sexologist;
Exclusion Criteria
1. A history of Childhood Sexual Abuse;
2. Subjects who had used testosterone therapy within 6 months before study entry;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To confirm the lack of effect of sublingual testosterone on physiological and subjective measures of sexual arousal in women with Hypoactive Sexual Desire Disorder (HSDD).
- Secondary Outcome Measures
Name Time Method To confirm the lack of effect of sublingual testosterone on physiological and subjective measures of sexual arousal at three post dose time points.<br><br>