The Impact of a Topical Vasodilating Cream on Female Sexual Experience (TVConFSD)
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ClinicalTrials.gov Identifier: NCT01078077
Verified March 2012 by Michael Pelekanos MD, East Suburban Ob Gyn. Recruitment status was: Recruiting
The purpose of this study is to determine if a topical vasodilating cream will improve female sexual experience.
Condition or disease
Female Sexual Dysfunction
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
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Ages Eligible for Study:
25 Years to 60 Years (Adult)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Sexually active females from ages 25 to sixty not on SSRI's without neurologic disease able sign and understand informed consent
Healthy females ages 25 to sixty sexually active
Neurologic disease, on SSRI's,advanced diabetes, non sexually active, mentally incompetent