Patient Satisfaction Survey of Non-surgical Urinary Incontinence Treatment

Completed

Conditions studied: Urinary Incontinence

In brief

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 acceptable symptom state (PASS) question to responses from other questionnaires regarding urinary symptoms.

Key facts

Study ID

NCT04064970

Run by

University of Rochester

People needed

125

Starts

2019-03-14

Expected to finish

2020-07-01

Last updated by the study team

2020-10-06

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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.

Where it is running

• University Urogynecology Associates — Rochester, New York, United States

Full record on ClinicalTrials.gov

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