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Postop Catheterization for Urinary Retention

Sponsor
NorthShore University HealthSystem (Other)
Overall Status
Terminated
CT.gov ID
NCT04030377
Collaborator
(none)
47
Enrollment
1
Location
58.7
Actual Duration (Months)
0.8
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This study investigates patient's preference and satisfaction with choice of catheterization after surgical urogynecological procedures.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Preoperatively, the enrolled patient receives information about risks and benefits of three ways of bladder catheterization as means of management of postoperative urinary retention. Based on this information, the patient chooses her preferred way of postoperative catheterization in case she experiences acute urinary retention after surgery. After the surgery, those patients requiring catheterization postoperatively evaluate their experience in a postoperative questionnaire.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    47 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Treatment of Postoperative Urinary Retention - WHAT DO WOMEN WANT?
    Actual Study Start Date :
    Apr 1, 2010
    Actual Primary Completion Date :
    Dec 1, 2014
    Actual Study Completion Date :
    Feb 20, 2015

    Outcome Measures

    Primary Outcome Measures

    1. Patient satisfaction with choice of catheterization method [2 weeks after index procedure]

      Assessed through post-operative questionnaire completion

    Secondary Outcome Measures

    1. Assessment of complication rates [2 weeks after index procedure]

      Comparison of complication rates between intermittent vs. indwelling catheterization: data derived from review of participant medical record

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • All female patients who undergo urogynecological surgery procedures at NorthShore University HealthSystem and consent to participate
    Exclusion Criteria:
    • Patients who cannot read, comprehend, and write in English

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 NorthShore University HealthSystem Skokie Illinois United States 60076

    Sponsors and Collaborators

    • NorthShore University HealthSystem

    Investigators

    • Study Director: Sylvia M Botros, MD, NorthShore University HealthSystem

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    NorthShore University HealthSystem
    ClinicalTrials.gov Identifier:
    NCT04030377
    Other Study ID Numbers:
    • EH11-096
    First Posted:
    Jul 24, 2019
    Last Update Posted:
    Jul 24, 2019
    Last Verified:
    Jul 1, 2019
    Additional relevant MeSH terms:
    Urinary Retention

    Study Results

    No Results Posted as of Jul 24, 2019