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Patient Satisfaction Survey of Non-surgical Urinary Incontinence Treatment

NCT04064970 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 125

Last updated 2020-10-06

No results posted yet for this study

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

Conditions

Interventions

BEHAVIORAL

patient acceptable symptom state (PASS)

The Severity Index for Urinary Incontinence, which documents incontinence frequency and severity, pelvic floor distress, patient global impression of severity and improvement, physical function, depression, sleep disturbance, anxiety, global health and ability to participate in social roles and activities.

Sponsors & Collaborators

  • University of Rochester

    lead OTHER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-03-14
Primary Completion
2020-07-01
Completion
2020-07-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04064970 on ClinicalTrials.gov