Uroflow Measurements in Urogynecology Patients Compared to Healthy Female Volunteers

Completed

• Conditions: Urogynecology

• Registration Number: NCT00919048
• Lead Sponsor: University of Rochester

Brief Summary

To compare uroflowmetry measurements of patients undergoing urodynamic testing as part of an incontinence work-up in an urogynecology practice to healthy female volunteers.

Detailed Description

Not available

Study Timeline

• Study Start: 2008-09
• Primary Completion: 2008-09
• Study Completion: 2008-09
• Study First Submitted: 2009-06-10
• Study First Submitted QC: 2009-06-11
• Study First Posted: 2009-06-12
• Status Verified: 2009-12
• Last Update Submitted: 2009-12-15
• Last Update Posted: 2009-12-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 36

Inclusion Criteria

• All patients who underwent urodynamics at the urogynecology clinic during the past 12 months
• Voids larger than 50 mls.

Exclusion Criteria

• History of pelvic organ prolapse, incomplete bladder emptying, and voids less than 50cc.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Voiding variables of patients will be compared to those of healthy female volunteers collected from another study.

Trial Locations

Locations (1)

University of Rochester; 🇺🇸 Rochester, New York, United States