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Uroflow Measurements in Urogynecology Patients Compared to Healthy Female Volunteers

This study has been completed.
Sponsor:
Information provided by:
University of Rochester
ClinicalTrials.gov Identifier:
NCT00919048
First received: June 10, 2009
Last updated: December 15, 2009
Last verified: December 2009
History of Changes
  Purpose

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


Condition
Urogynecology

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Uroflow Measurements in Urogynecology Patients Compared to Healthy Female Volunteers

Further study details as provided by University of Rochester:

Primary Outcome Measures:
  • Voiding variables of patients will be compared to those of healthy female volunteers collected from another study. [ Designated as safety issue: No ]

Estimated Enrollment: 36
Study Start Date: September 2008
Study Completion Date: September 2008
Primary Completion Date: September 2008 (Final data collection date for primary outcome measure)
Groups/Cohorts
Urodynamic patients
Uroflow studies of patients who underwent urodynamics as part of an incontinence work-up.

  Eligibility

Ages Eligible for Study:   25 Years to 60 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Urogynecology clinic

Criteria

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.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00919048

Locations
United States, New York
University of Rochester
Rochester, New York, United States, 14642
Sponsors and Collaborators
University of Rochester
Investigators
Principal Investigator: Gunhilde Buchsbaum, MD University of Rochester
  More Information

No publications provided

Responsible Party: Gunhilde Buchsbaum, MD, University of Rochester
ClinicalTrials.gov Identifier: NCT00919048     History of Changes
Other Study ID Numbers: 25597
Study First Received: June 10, 2009
Last Updated: December 15, 2009
Health Authority: United States: Institutional Review Board

ClinicalTrials.gov processed this record on May 19, 2013