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Uroflow Measurements in Urogynecology Patients Compared to Healthy Female Volunteers

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ClinicalTrials.gov Identifier: NCT00919048
Recruitment Status : Completed
First Posted : June 12, 2009
Last Update Posted : December 16, 2009
Sponsor:
Information provided by:

Study Description
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.

Condition or disease
Urogynecology

Study Design

Study Type : Observational
Estimated Enrollment : 36 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Uroflow Measurements in Urogynecology Patients Compared to Healthy Female Volunteers
Study Start Date : September 2008
Primary Completion Date : September 2008
Study Completion Date : September 2008
Groups and Cohorts

Group/Cohort
Urodynamic patients
Uroflow studies of patients who underwent urodynamics as part of an incontinence work-up.


Outcome Measures

Primary Outcome Measures :
  1. Voiding variables of patients will be compared to those of healthy female volunteers collected from another study.

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   25 Years to 60 Years   (Adult)
Sexes 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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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

Responsible Party: Gunhilde Buchsbaum, MD, University of Rochester
ClinicalTrials.gov Identifier: NCT00919048     History of Changes
Other Study ID Numbers: 25597
First Posted: June 12, 2009    Key Record Dates
Last Update Posted: December 16, 2009
Last Verified: December 2009