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Uroflow Measurements in Urogynecology Patients Compared to Healthy Female Volunteers

Sponsor
University of Rochester (Other)
Overall Status
Completed
CT.gov ID
NCT00919048
Collaborator
(none)
36
Enrollment
1
Location

Study Details

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 Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    36 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Uroflow Measurements in Urogynecology Patients Compared to Healthy Female Volunteers
    Study Start Date :
    Sep 1, 2008
    Actual Primary Completion Date :
    Sep 1, 2008
    Actual Study Completion Date :
    Sep 1, 2008

    Arms and Interventions

    Arm Intervention/Treatment
    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

    Criteria

    Ages Eligible for Study:
    25 Years to 60 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    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

    Locations

    Site City State Country Postal Code
    1 University of Rochester Rochester New York United States 14642

    Sponsors and Collaborators

    • University of Rochester

    Investigators

    • Principal Investigator: Gunhilde Buchsbaum, MD, University of Rochester

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00919048
    Other Study ID Numbers:
    • 25597
    First Posted:
    Jun 12, 2009
    Last Update Posted:
    Dec 16, 2009
    Last Verified:
    Dec 1, 2009

    Study Results

    No Results Posted as of Dec 16, 2009