The Impact of a Topical Vasodilating Cream on Female Sexual Experience
- Conditions
- Female Sexual Dysfunction
- Registration Number
- NCT01078077
- Lead Sponsor
- Michael Pelekanos MD
- Brief Summary
The purpose of this study is to determine if a topical vasodilating cream will improve female sexual experience.
- Detailed Description
To determine in a placebo controlled double blinded study whether a topically applied vasodilating cream will improve the female sexual response as measured by a standard female sexual dysfunction questionnaire
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
- Healthy females ages 25 to sixty sexually active
Exclusion Criteria
- Neurologic disease, on SSRI's,advanced diabetes, non sexually active, mentally incompetent
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (3)
East Suburban Obgyn
πΊπΈMonroeville, Pennsylvania, United States
West Penn Allegheny Health Center
πΊπΈMonroeville, Pennsylvania, United States
West Penn Hospital Forbes Campus
πΊπΈMonroeville, Pennsylvania, United States
East Suburban ObgynπΊπΈMonroeville, Pennsylvania, United StatesMichael J Pelekanos, MDPrincipal InvestigatorGuy Stoffman, MDContact412 3706313guystof@aol.com
