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Duration of Stay After Urologic Surgery : Neuraxial Versus General Anesthesia

Sponsor
University Hospital, Strasbourg, France (Other)
Overall Status
Unknown status
CT.gov ID
NCT03517202
Collaborator
(none)
260
Enrollment
1
Location
2.6
Anticipated Duration (Months)
98.9
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Outpatient midurethral surgery is a frequent surgery. It is performed either under general anesthesia or neuraxial anesthesia. A frequent complication is postoperative urinary retention requiring urinary catheterization, which implies a higher infectious risk.

The investigators compared the complication rate after TVT surgery depending on the type of anesthesia.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    260 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Duration of Stay for Outpatient Surgery After Tension Free Vaginal Tape (TVT) Urologic Surgery : Neuraxial Versus General Anesthesia
    Actual Study Start Date :
    Mar 13, 2018
    Anticipated Primary Completion Date :
    Jun 1, 2018
    Anticipated Study Completion Date :
    Jun 1, 2018

    Outcome Measures

    Primary Outcome Measures

    1. The investigators compared the rate of complications after TVT surgery depending on the type of anesthesia and the need for urinary catheterization, requiring longer hospital stay after surgery. [The period from January 1st, 2012 to December 31st, 2016 will be examined]

      Patients hospitalized at Strasbourg University Hospital from 2012 to 2016.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    • Age > 18 years

    • Sex: Female

    • Patient who has consented to the use of her medical data for research purposes.

    • Patient undergoing outpatient urinary incontinence surgery using TVT between 2012 and 2016

    Exclusion Criteria:

    • Specific clinical forms of the disease,

    • Interfering treatments and associated diseases, history,

    • Refusal of the patient to participate in the study

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Service d'Anesthésiologie - Réanimation Strasbourg France 67091

    Sponsors and Collaborators

    • University Hospital, Strasbourg, France

    Investigators

    • Principal Investigator: Valentina FAITOT, MD, University Hospital, Strasbourg, France

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Strasbourg, France
    ClinicalTrials.gov Identifier:
    NCT03517202
    Other Study ID Numbers:
    • 7001
    First Posted:
    May 7, 2018
    Last Update Posted:
    Jun 4, 2018
    Last Verified:
    Mar 1, 2018
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University Hospital, Strasbourg, France
    Urologic surgery
    Urinary incontinence
    Tension Free Vaginal Tape
    Post-operative urinary retention
    Outpatient surgery
    Additional relevant MeSH terms:
    Urinary Retention

    Study Results

    No Results Posted as of Jun 4, 2018