Trial Comparing TVT SECUR System and Trans Vaginal Obturator Tape for Surgical Management of Stress Urinary Incontinence
Primary Purpose
Stress Urinary Incontinence
Status
Terminated
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
transvaginal obturator tape
Sponsored by
About this trial
This is an interventional treatment trial for Stress Urinary Incontinence
Eligibility Criteria
Inclusion Criteria:
- Female patients with symptoms of stress urinary incontinence and a positive cough test who require surgical management. Cough test is positive when leakage of urine is seen from the urethra synchronously with the patient performing a cough or valsalva manuver with a comfortably full bladder in the lying or standing position.
Exclusion Criteria:
- Women with predominantly symptoms of urge urinary incontinence
- Presence of prolapse greater than Pelvic organ prolapse quantification (POPQ) Stage 1 or prolapse requiring surgery
- Detrusor overactivity on cystometrogram at urodynamic testing
- Previous surgery for incontinence
- Intrinsic sphincter deficiency (MUCP<20 cm H2O or Q -tip <30o)
- Voiding dysfunction with postvoid residual >100 cc
Sites / Locations
- St. Boniface Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
TVT SECURE
TVT O
Arm Description
sling
sling
Outcomes
Primary Outcome Measures
Objective cure as defined by the cough test at one year from surgery
Secondary Outcome Measures
Full Information
NCT ID
NCT00527696
First Posted
September 10, 2007
Last Updated
January 8, 2016
Sponsor
University of Manitoba
1. Study Identification
Unique Protocol Identification Number
NCT00527696
Brief Title
Trial Comparing TVT SECUR System and Trans Vaginal Obturator Tape for Surgical Management of Stress Urinary Incontinence
Official Title
Randomized Clinical Trial Comparing TVT SECUR System (TVT S) and Trans Vaginal Obturator Tape (TVT-O) for Surgical Management of Stress Urinary Incontinence
Study Type
Interventional
2. Study Status
Record Verification Date
January 2016
Overall Recruitment Status
Terminated
Why Stopped
statistical Significance was reached for primary outcome
Study Start Date
May 2008 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
October 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Manitoba
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To compare the efficacy and complications of the TVT SECUR system (TVT S) and trans-vaginal obturator tape (TVT-O) procedures for the surgical management of female stress urinary incontinence.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stress Urinary Incontinence
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
106 (Actual)
8. Arms, Groups, and Interventions
Arm Title
TVT SECURE
Arm Type
Active Comparator
Arm Description
sling
Arm Title
TVT O
Arm Type
Active Comparator
Arm Description
sling
Intervention Type
Procedure
Intervention Name(s)
transvaginal obturator tape
Primary Outcome Measure Information:
Title
Objective cure as defined by the cough test at one year from surgery
Time Frame
one year
10. Eligibility
Sex
Female
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Female patients with symptoms of stress urinary incontinence and a positive cough test who require surgical management. Cough test is positive when leakage of urine is seen from the urethra synchronously with the patient performing a cough or valsalva manuver with a comfortably full bladder in the lying or standing position.
Exclusion Criteria:
Women with predominantly symptoms of urge urinary incontinence
Presence of prolapse greater than Pelvic organ prolapse quantification (POPQ) Stage 1 or prolapse requiring surgery
Detrusor overactivity on cystometrogram at urodynamic testing
Previous surgery for incontinence
Intrinsic sphincter deficiency (MUCP<20 cm H2O or Q -tip <30o)
Voiding dysfunction with postvoid residual >100 cc
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ken D Maslow, MD
Organizational Affiliation
St. Boniface Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Boniface Hospital
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R2H 2A6
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
24452619
Citation
Maslow K, Gupta C, Klippenstein P, Girouard L. Randomized clinical trial comparing TVT Secur system and trans vaginal obturator tape for the surgical management of stress urinary incontinence. Int Urogynecol J. 2014 Jul;25(7):909-14. doi: 10.1007/s00192-013-2312-7. Epub 2014 Jan 23.
Results Reference
derived
Learn more about this trial
Trial Comparing TVT SECUR System and Trans Vaginal Obturator Tape for Surgical Management of Stress Urinary Incontinence
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