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@home: a study to investigate the subjective and physiological efficacy and safety of Lybrido and Lybridos in the domestic setting in healthy female subjects with Female Sexual Dysfunction and SSRI usage.

Recruiting
Conditions
Selective serotonin reuptake inhibitors (SSRIs), Female sexual dysfunction (FSD), Hypoactive sexual desire disorder, Female sexual arousal disorder
Registration Number
NL-OMON23989
Lead Sponsor
Emotional Brain BV
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

1. Provision of written informed consent;

2. Female 21 – 70 years of age with Hypoactive Sexual Desire Disorder (comorbidity with other sexual dysfunctions e.g Female Sexual Arousal Disorder (FSAD) is allowed) and/or SSRI induced sexual dysfunctioning. The diagnosis will be made by an experienced psychologist/sexologist;

Exclusion Criteria

1. Use of oral contraception containing anti-androgens (Like Diane 35 or Minerva);

2. Use of oral contraception containing 50 μg estrogen or more;

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate efficacy of Lybrido and Lybridos on subjective sexual experience in the domestic setting in healthy female subjects Female Sexual Dysfunction using SSRIs.
Secondary Outcome Measures
NameTimeMethod
1. To evaluate efficacy of Lybrido and Lybridos on physiological sexual responding (vaginal and clitoral) in the domestic setting in different subgroups of women with FSD in combination with SSRI use;<br /><br>2. To investigate differences in attentional bias for erotic stimuli in different subgroups of women with FSD and SSRI induced FSD, and the influence of Lybrido and Lybridos herein;<br /><br>3. To investigate differences in subjective, physiological and neuropsychological responding at home or in the laboratory;<br /><br>4. To evaluate the safety of Lybrido and Lybridos in the domestic setting.
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