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Trans-obturator Mid-urethral Sling and the Single-incision Sling in Women With Stress Urinary Incontinence

Primary Purpose

Urinary Incontinence, Stress

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
TOT - inside-out trans-obturator tape/sling
SIS - Innovative fixation single incision sling
Sponsored by
Brno University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Incontinence, Stress

Eligibility Criteria

35 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

Women with pure or predominant urodynamic stress urinary incontinence confirmed during filling cystometry by positive standardized cough stress test (CST) with urinary bladder filling of 250 ml in lithotomy position.

Exclusion Criteria:

  • patients with predominant urge incontinence
  • patients with intrinsic sphincter deficiency (MUCP<20 cmH2O)
  • pelvic organ prolapse (POP-Q>2)
  • previous urinary incontinence surgery
  • previous pelvic organ prolapse surgery
  • presence of other pelvic organ pathology.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    SIS single incision sling

    TOT trans obturator tape/sling

    Arm Description

    SIS - Innovative fixation single incision sling A third generation of the Mid-urethral slings inserted through a SIS single incision sling (SIS) to treat female stress urinary incontinence (SUI).

    TOT - inside-out trans-obturator tape/sling Trans-obturator slings (TOT) now represent a gold standard in the treatment of female stress urinary incontinence (SUI).

    Outcomes

    Primary Outcome Measures

    Percentage of Participants With Negative Cough Stress Test (CST)
    Negative cough stress test four years after incontinence surgery.
    Patient Global Impression of Improvement (PGI-I) Score
    Patient Global Impression of Improvement (PGI-I) score four years after incontinence surgery. The Patient Global Impression of Improvement (PGI-I) is a global index that may be used to rate the response of a condition to a therapy (transition scale). It is a simple, direct, easy to use scale that is intuitively understandable to clinicians Very much better Much better A little better No change A little worse Much worse Very much worse

    Secondary Outcome Measures

    Number of Participants With Major Perioperative Complications
    Number of Participants With Major Postoperative Complications

    Full Information

    First Posted
    July 21, 2015
    Last Updated
    February 10, 2020
    Sponsor
    Brno University Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02506309
    Brief Title
    Trans-obturator Mid-urethral Sling and the Single-incision Sling in Women With Stress Urinary Incontinence
    Official Title
    Prospective Randomized Comparison of the Trans-obturator Mid-urethral Sling and the Single-incision Sling in Women With Stress Urinary Incontinence
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2020
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2015 (Actual)
    Primary Completion Date
    December 2015 (Actual)
    Study Completion Date
    December 2019 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Brno University Hospital

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Mid-urethral slings (MUS) now represent a gold standard in the treatment of female stress urinary incontinence (SUI). Second generation trans-obturator slings (TOT) have proven to be as effective as retropubic tension-free vaginal tape (TVT) with fewer major complications. A third generation of the MUS inserted through a single vaginal incision (SIS) has become a means to overcome significant post-operative groin pain. Novel types of SIS with a more robust and adjustable anchoring mechanism can assure adequate long-lasting attachment to the obturator membrane (OM). Objective of this study was to compare an inside-out TOT with an innovative fixation SIS in randomized controlled trial on patients undergoing their primary surgery for urodynamic SUI.
    Detailed Description
    Objective of this study was to compare an inside-out TOT (Gynecare TVT Obturator System, Ethicon) with an innovative fixation SIS (Ophira, Promedon) in randomized controlled trial on patients undergoing their primary surgery for urodynamic SUI. A prospective randomized controlled trial (RCT) is performed in one tertiary referral urogynecology center from January 2015 thru December 2015. Study included women with pure or predominant urodynamic SUI confirmed during cystometry by positive standardized cough stress test (CST) with urinary bladder filling of 250 ml in lithotomy position. Study was carried out on a Caucasian Czech (central European) population. A study power analysis was calculated with an expected objective cure rate of minimum 80 % for both patient groups, false non-match rate (alpha) of 0.05, and false match rate (beta) of 0.10. A minimum sample size of 80 patients was required for each group.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Urinary Incontinence, Stress

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    168 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    SIS single incision sling
    Arm Type
    Experimental
    Arm Description
    SIS - Innovative fixation single incision sling A third generation of the Mid-urethral slings inserted through a SIS single incision sling (SIS) to treat female stress urinary incontinence (SUI).
    Arm Title
    TOT trans obturator tape/sling
    Arm Type
    Active Comparator
    Arm Description
    TOT - inside-out trans-obturator tape/sling Trans-obturator slings (TOT) now represent a gold standard in the treatment of female stress urinary incontinence (SUI).
    Intervention Type
    Device
    Intervention Name(s)
    TOT - inside-out trans-obturator tape/sling
    Other Intervention Name(s)
    Gynecare TVT Obturator System (Ethicon)
    Intervention Description
    Patients were randomized by envelope technique at the time of surgery indication to either TOT or SIS anti-incontinence surgical procedure with mid-urethral slings (MUS)
    Intervention Type
    Device
    Intervention Name(s)
    SIS - Innovative fixation single incision sling
    Other Intervention Name(s)
    Ophira (Promedon)
    Intervention Description
    Patients were randomized by envelope technique at the time of surgery indication to either TOT or SIS anti-incontinence surgical procedure with mid-urethral slings (MUS)
    Primary Outcome Measure Information:
    Title
    Percentage of Participants With Negative Cough Stress Test (CST)
    Description
    Negative cough stress test four years after incontinence surgery.
    Time Frame
    four years
    Title
    Patient Global Impression of Improvement (PGI-I) Score
    Description
    Patient Global Impression of Improvement (PGI-I) score four years after incontinence surgery. The Patient Global Impression of Improvement (PGI-I) is a global index that may be used to rate the response of a condition to a therapy (transition scale). It is a simple, direct, easy to use scale that is intuitively understandable to clinicians Very much better Much better A little better No change A little worse Much worse Very much worse
    Time Frame
    four years
    Secondary Outcome Measure Information:
    Title
    Number of Participants With Major Perioperative Complications
    Time Frame
    one month
    Title
    Number of Participants With Major Postoperative Complications
    Time Frame
    four years

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    35 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Women with pure or predominant urodynamic stress urinary incontinence confirmed during filling cystometry by positive standardized cough stress test (CST) with urinary bladder filling of 250 ml in lithotomy position. Exclusion Criteria: patients with predominant urge incontinence patients with intrinsic sphincter deficiency (MUCP<20 cmH2O) pelvic organ prolapse (POP-Q>2) previous urinary incontinence surgery previous pelvic organ prolapse surgery presence of other pelvic organ pathology.

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    21412819
    Citation
    Ogah J, Cody DJ, Rogerson L. Minimally invasive synthetic suburethral sling operations for stress urinary incontinence in women: a short version Cochrane review. Neurourol Urodyn. 2011 Mar;30(3):284-91. doi: 10.1002/nau.20980.
    Results Reference
    background
    PubMed Identifier
    24880654
    Citation
    Nambiar A, Cody JD, Jeffery ST. Single-incision sling operations for urinary incontinence in women. Cochrane Database Syst Rev. 2014 Jun 1;(6):CD008709. doi: 10.1002/14651858.CD008709.pub2.
    Results Reference
    background

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    Trans-obturator Mid-urethral Sling and the Single-incision Sling in Women With Stress Urinary Incontinence

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