Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02862184

Female Sexual Dysfunction, Risks and Outcomes (FSFI)

Status
Withdrawn
Phase
Study type
Observational
Enrollment
0 (actual)
Sponsor
St. Louis University · Academic / Other
Sex
Female
Age
18 Years – 89 Years
Healthy volunteers
Not accepted

Summary

Many women will likely experience a sexual problem in their lifetimes. The Prevalence of Female Sexual Problems Associated with Distress and Determinants of Treatment Seeking (PRESIDE) study surveyed more than 30,000 U.S. women aged \>18 years regarding sexual function. Results from this study estimated that 12% of women experience a diagnosable sexual disorder that causes personal distress, with lack of sexual desire being the most prevalent. - See more at: http://www.uspharmacist.com/content/d/featured\_articles/c/56908/#sthash.LTDkyRlR.dpuf

Detailed description

Standard of care includes completion of a sexual dysfunctional questionnaire at every visit. This study will collect information from the questionnaires and office visit and follow the patient for outcomes of successful or non successful treatment. The purpose of this study is to collect and analyze data on the characteristics of women who present with sexual dysfunction, to evaluate what risk factors contribute to sexual dysfunction and to evaluate what factors contribute to successful treatment of sexual dysfunction. Upon a visit to the office participants will complete the Female Sexual Function Index (FSFI), this is standard of care for all patients. Research related procedures include: Review of questionnaires and collecting data from medical records regarding medical history, and treatment outcomes. If a participant does not return to the office for a follow up visit (or final visit) the final questionnaire will be sent by their preference (e-mail, phone, or mail) noted in the consent form. Participates will also be given the option of participating in a "future storage of data". Future testing will be in the area of female sexual dysfunction. Data will be identified by a code number and only the research staff at Saint Louis University will have access to the data.

Conditions

Timeline

Start date
2016-07-01
Primary completion
2017-01-01
Completion
2017-01-01
First posted
2016-08-10
Last updated
2017-01-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02862184. Inclusion in this directory is not an endorsement.