Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
OBSERVATIONAL
2016-07-31
2017-01-31
Brief Summary
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Detailed Description
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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
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
\-
18 Years
89 Years
FEMALE
No
Sponsors
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St. Louis University
OTHER
Responsible Party
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Becky Lynn, MD
Assistant Professor
Principal Investigators
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Becky Lynn, MD
Role: PRINCIPAL_INVESTIGATOR
St. Louis University
Locations
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St. Mary's Health Center
St Louis, Missouri, United States
Countries
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Other Identifiers
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26311
Identifier Type: -
Identifier Source: org_study_id
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