Trial Comparing Mini-Arc Precise Pro and the Trans Vaginal Obturator Tape for Stress Urinary Incontinence
Primary Purpose
Stress Urinary Incontinence, Urethral Sling Surgery
Status
Unknown status
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Mini Arc Precise Pro and Trans vaginal obturator sling (TVT-0)
Sponsored by
About this trial
This is an interventional treatment trial for Stress Urinary Incontinence
Eligibility Criteria
Inclusion Criteria:
- women with stress urinary incontinence with a positive cough test
- patient request surgery for treatment
Exclusion Criteria:
- prodominantely overactive bladder
- previous failed procedure
- MUCP <20 cm H2O
- presence of vaginal prolapse > stage 1
- voiding dysfunction (PVR>100 mL)
Sites / Locations
- Ken Maslow
Arms of the Study
Arm 1
Arm Type
Active Comparator
Arm Label
Precise sling vs TVT-O sling
Arm Description
Outcomes
Primary Outcome Measures
Cough test at one year from surgery
Secondary Outcome Measures
Subjective symptoms, QOL questionaires
Full Information
NCT ID
NCT01799122
First Posted
February 22, 2013
Last Updated
January 8, 2016
Sponsor
University of Manitoba
1. Study Identification
Unique Protocol Identification Number
NCT01799122
Brief Title
Trial Comparing Mini-Arc Precise Pro and the Trans Vaginal Obturator Tape for Stress Urinary Incontinence
Official Title
Randomized Clinical Trial Comparing Mini-Arc Precise Pro and the Trans Vaginal Obturator Tape for Surgical Management of Stress Urinary Incontinence
Study Type
Interventional
2. Study Status
Record Verification Date
January 2016
Overall Recruitment Status
Unknown status
Study Start Date
undefined (undefined)
Primary Completion Date
February 2017 (Anticipated)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Manitoba
4. Oversight
5. Study Description
Brief Summary
Randomized comparison of two surgeries for the treatment 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, Urethral Sling Surgery
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
8. Arms, Groups, and Interventions
Arm Title
Precise sling vs TVT-O sling
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
Mini Arc Precise Pro and Trans vaginal obturator sling (TVT-0)
Primary Outcome Measure Information:
Title
Cough test at one year from surgery
Time Frame
One year
Secondary Outcome Measure Information:
Title
Subjective symptoms, QOL questionaires
Time Frame
1 & 2 years post surgery
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
women with stress urinary incontinence with a positive cough test
patient request surgery for treatment
Exclusion Criteria:
prodominantely overactive bladder
previous failed procedure
MUCP <20 cm H2O
presence of vaginal prolapse > stage 1
voiding dysfunction (PVR>100 mL)
Facility Information:
Facility Name
Ken Maslow
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R2H 2A6
Country
Canada
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ken D Maslow, MD
Phone
204-235-3039
Email
kmaslow@sbgh.mb.ca
12. IPD Sharing Statement
Learn more about this trial
Trial Comparing Mini-Arc Precise Pro and the Trans Vaginal Obturator Tape for Stress Urinary Incontinence
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