Uroflow Measurements in Urogynecology Patients Compared to Healthy Female Volunteers

Urogynecology Clinical Trial

Official title:

Uroflow Measurements in Urogynecology Patients Compared to Healthy Female Volunteers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00919048
• Other study ID #: 25597
• Status: Completed
• Phase: N/A
• First received: June 10, 2009
• Last updated: December 15, 2009
• Start date: September 2008
• Est. completion date: September 2008

Study information

• Verified date: December 2009
• Source: University of Rochester
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 36
• Est. completion date: September 2008
• Est. primary completion date: September 2008
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 25 Years to 60 Years

Eligibility

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

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Urogynecology

Locations

Country	Name	City	State
United States	University of Rochester	Rochester	New York

Sponsors (1)

Lead Sponsor	Collaborator
University of Rochester

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Voiding variables of patients will be compared to those of healthy female volunteers collected from another study.			No