Status:
COMPLETED
Evaluate Women After Vaginal Surgery for Urinary Symptoms and Sexual Function
Lead Sponsor:
Corewell Health East
Conditions:
Urinary Incontinence
Pelvic Organ Prolapse
Eligibility:
FEMALE
18+ years
Brief 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 F...
Eligibility Criteria
Inclusion
- Women at least 18 years of age
- Having urinary incontinence or pelvic organ prolapse
- Capable of giving informed consent
- Capable and willing to follow all study related procedures
Exclusion
- Reported history of urethral obstruction (not secondary to prolapse), stricture, bladder calculi or bladder tumor in the last 2 years.
- Pregnant as confirmed by urine pregnancy test or plans to become pregnant during the study period.
- Breast feeding
- Currently participating or have participated within the past 30 days in any clinical investigation involving or impacting urinary or renal function
- Cannot independently comprehend and complete the questionnaires.
- The subject is deemed unsuitable for enrollment in this study by the investigators based on their history or physical examination.
Key Trial Info
Start Date :
August 1 2006
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
January 1 2009
Estimated Enrollment :
41 Patients enrolled
Trial Details
Trial ID
NCT00376441
Start Date
August 1 2006
End Date
January 1 2009
Last Update
August 23 2011
Active Locations (1)
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1
William Beaumont Hospital
Royal Oak, Michigan, United States, 48073