Clinical Trials Directory

Trials / Completed

CompletedNCT00376441

Evaluate Women After Vaginal Surgery for Urinary Symptoms and Sexual Function

Study of Sexual Function and Urinary Symptoms in Women Having Vaginal Surgeries

Status
Completed
Phase
Study type
Observational
Enrollment
41 (actual)
Sponsor
Corewell Health East · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

Assess the outcomes of vaginal surgeries and its impact on sexual function and urinary symptoms.

Detailed description

Currently, up to 43% of women in the United States have female sexual dysfunction (FSD). In a recent study of 109 sexually active women in a urogynecology practice, FSD was noted using the validated Female Sexual Function Index (FSFI) in 64% of the women. Difficulties with sexual function are also associated with pelvic organ prolapse and urinary incontinence. One in nine women will have surgery for incontinence or prolapse in her lifetime. The impact of vaginal surgeries on sexual function and urinary symptoms has been scarcely reported in the literature. The methodology of most of those studies is flawed by the use of questionnaires that were not validated, small sample sizes and no comparison control group. In addition, several studies only focused on one surgical intervention, specific types of incontinence or prolapse, or both. It is difficult to make sense out of the discordant research findings when applying it to our patient population. This is a prospective study of women with incontinence or pelvic organ prolapse. Subjects will be selected from three urology practices. All patients will be asked to complete a short patient history form. If the woman meets the study criteria, the study will be explained and if she agrees to participate in this study, informed consent will be obtained. She will then complete the FSFI, SF-12 and PFDI-20 questionnaires.

Conditions

Interventions

TypeNameDescription
PROCEDUREVaginal Surgerypatients undergoing vaginal surgery

Timeline

Start date
2006-08-01
Primary completion
2008-12-01
Completion
2009-01-01
First posted
2006-09-14
Last updated
2011-08-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00376441. Inclusion in this directory is not an endorsement.