Retrospective Evaluation of the Effect of Ultrasound-guided Obturator Nerve Block on Complications in Transurethral (TUR-M) Resection Surgery for Bladder Side Wall Tumors.

Sponsor
Erol Olcok Corum Training and Research Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04995445
Collaborator
(none)
115
1
26.2
4.4

Study Details

Study Description

Brief Summary

In this study, the effectiveness of obturator nerve block added to spinal anesthesia in the operation of transurethral resection (TUR-M) of bladder lateral-infrolateral wall tumors on the obturator reflex and related complications was investigated.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    115 participants
    Observational Model:
    Other
    Time Perspective:
    Retrospective
    Official Title:
    Retrospective Evaluation of the Effect of Ultrasound-guided Obturator Nerve Block on Complications in Transurethral (TUR-M) Resection Surgery for Bladder Side Wall Tumors.
    Actual Study Start Date :
    Apr 26, 2019
    Actual Primary Completion Date :
    Jan 20, 2021
    Actual Study Completion Date :
    Jul 1, 2021

    Outcome Measures

    Primary Outcome Measures

    1. Effect of ultrasound-guided obturator nerve block on complications in transurethral resection of bladder cancer [2 year]

      patient who underwent spinal anesthesia and obturator block

    Secondary Outcome Measures

    1. Effect of ultrasound-guided obturator nerve block on complications in transurethral resection of bladder cancer [2 year]

      The patient group who underwent spinal anesthesia and obturator block and the group without obturator block

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    retrospective study

    Inclusion criteria:
    • Patients over the age of 18 who have undergone bladder tumor surgery and whose anesthesia method is spinal anesthesia
    Exclusion Criteria:
    • under 18 years old , received general anesthesia pregnant and pediatric patient data not used

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Çorum training and research state hospital Çorum Turkey 19030

    Sponsors and Collaborators

    • Erol Olcok Corum Training and Research Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    HULYA TOPCU, assistant professor, Erol Olcok Corum Training and Research Hospital
    ClinicalTrials.gov Identifier:
    NCT04995445
    Other Study ID Numbers:
    • 2019-158
    First Posted:
    Aug 9, 2021
    Last Update Posted:
    Aug 9, 2021
    Last Verified:
    Aug 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by HULYA TOPCU, assistant professor, Erol Olcok Corum Training and Research Hospital

    Study Results

    No Results Posted as of Aug 9, 2021