Status:
COMPLETED
Patient Satisfaction Survey of Non-surgical Urinary Incontinence Treatment
Lead Sponsor:
University of Rochester
Conditions:
Urinary Incontinence
Eligibility:
FEMALE
18+ years
Brief Summary
The purpose of this study is to identify self-reported wellness following nonsurgical treatment of stress urinary incontinence. This will be done by correlating the response of "yes" on the patient ac...
Eligibility Criteria
Inclusion
- Adult women (\> 18 years) seeking care for stress urinary incontinence at the URMC in Rochester, NY, DUMC in Durham, NC, Western New York (WNY) Urology Associates in Cheektowaga, NY, or at the UTMB in Galveston, TX.
- English-speaking
- Possess the ability to complete electronic patient reported outcome questionnaires and voiding diaries
Exclusion
- Women who decline to participate in the study
- Women were unable to complete electronic patient reported outcome questionnaires
- Women with greater than stage II uterovaginal prolapse or post-hysterectomy prolapse.
- Women considered citizens of the European Union (EU), including EU citizens living in the United States.
Key Trial Info
Start Date :
March 14 2019
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
July 1 2020
Estimated Enrollment :
125 Patients enrolled
Trial Details
Trial ID
NCT04064970
Start Date
March 14 2019
End Date
July 1 2020
Last Update
October 6 2020
Active Locations (1)
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1
University Urogynecology Associates
Rochester, New York, United States, 14623