The Impact of a Topical Vasodilating Cream on Female Sexual Experience

The Impact of a Topical Vasodilating Cream (When Applied to the Clitoris) on the Female Sexual Experience Using a Standard 7 Part Female Sexual Dysfunction Questionnaire

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01078077

Acronym

TVConFSD

Enrollment

200

Registered

2010-03-02

Start date

2010-03-31

Completion date

2012-07-31

Last updated

2012-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Female Sexual Dysfunction

Keywords

healthy females ages twentyfive through sixty

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

Interventions

None listed

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

25 Years to 60 Years

Healthy volunteers

Yes

Inclusion criteria

* Healthy females ages 25 to sixty sexually active

Exclusion criteria

* Neurologic disease, on SSRI's,advanced diabetes, non sexually active, mentally incompetent

Countries

United States

Contacts

Primary Contactmichael j pelekanos, MD

mipels@aol.com4128567500

Backup ContactGuy Stofman, MD

guystof@aol.com4123706313

Outcome results