Feasibility of Comparing Two Surgical Treatment of Female Urodynamic Stress (SITOT)
Primary Purpose
Female Stress Incontinence
Status
Completed
Phase
Phase 1
Locations
United Kingdom
Study Type
Interventional
Intervention
sub-urethral tape (TVT-O)
stand standard mid-urethral sling (TVT-O)
Sponsored by
About this trial
This is an interventional treatment trial for Female Stress Incontinence focused on measuring urodynamic urinary incontinence, sub-urethral tape
Eligibility Criteria
Inclusion Criteria:
- USI
- Mixed incontinence symptoms with predominantly bothering stress component (No DO on UDS).
- Primary Incontinence Surgery.
- BMI < 35
- Ability to understand the information leaflet and sign an informed consent form in English.
- All would have had failed or declined PFMT.
Exclusion Criteria:
- Mixed incontinence with pre-dominant OAB and/or Neurological conditions e.g. MS.
- Detrusor Overactivity on Urodynamics.
- Inability to understand English.
- Un-willing for randomisation.
- Concomitant surgery.
- Patient requiring postoperative hospital-stay for medical or social reasons
Sites / Locations
- (Grampian) Aberdeen Royal Infermary
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Single-incision Mini-slings (SIMS- Ajust)
standared med urethral sling (SMUS)
Arm Description
AjustTM has polypropylene fixing anchors (one is fixed and the other adjustable) which are anchored onto the obturator membrane. The pulley like system enables adjustment of the tension once the arms have been anchored. Once in place, the anchors rest at right angles to insertion which is claimed to reduce the chances of anchor dislodgment
standard med urethral sling (SMUS)TVT-O, was done as originally described by Deleval et al.
Outcomes
Primary Outcome Measures
• Feasibility of the single incision sub-urethral tape to be done under local anaesthesia
Feasibility of the single incision sub-urethral tape to be done under local anaesthesia?
Number of women approached and declining LA o Number of women in LA group converted to GA
Secondary Outcome Measures
• Patient-reported Success rates
Patient-reported Success rates
o Assessed by PGI-I "Very Much Improved/ Much Improved."
Full Information
NCT ID
NCT01230450
First Posted
October 27, 2010
Last Updated
January 23, 2013
Sponsor
University of Aberdeen
Collaborators
Aberdeen Royal Infirmary
1. Study Identification
Unique Protocol Identification Number
NCT01230450
Brief Title
Feasibility of Comparing Two Surgical Treatment of Female Urodynamic Stress
Acronym
SITOT
Official Title
Feasibility of Comparing Two Surgical Treatment of Female Urodynamic Stress Incontinence (SITOT)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
November 2009 (undefined)
Primary Completion Date
October 2010 (Actual)
Study Completion Date
October 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aberdeen
Collaborators
Aberdeen Royal Infirmary
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Aim: The study aim to assess the feasibly a large prospective multi-centre randomised study for comparing the relatively new "Single incision sub-urethral tapes" with the standard surgical treatment of female urodynamic stress incontinence (USI).
Detailed Description
Single incision tension-free sub-urethral vaginal tapes procedures8 have been recently described in an attempt to avoid the blind passage of the trochars through the groin & the adductor muscles and consequently reducing the incidence & severity of postoperative leg pain. The obvious advantages would be shorter hospital stay, early recovery, early resumption of day to day activities & earlier return to work. A number of small prospective audits and case-series have been presented in international conferences reporting on the safety & outcomes for these procedures. However all these studies were for preliminary reports for proof of concept and therefore the studies populations were 15-70 women with short term follow-up of 2-3 month9-11.These studies have shown low perioperative complication rates: bladder injury 0-1%, vaginal erosion 1-3% & one study showing 1.3% pain at 6 weeks follow-up. The patient reported success rates were 77-93% at 2-3 month follow-up9-12.
Objectives:
Establish the feasibility of the "Single incision sub-urethral tapes" to be done under local anaesthesia.
The feasibility of randomisation to the standard surgical treatment TVT-O / TVT.
To compare the surgical approach in this relatively new procedure against the standard procedures as regard: Peri-operative complication rates, Postoperative pain, Time to discharge from the hospital,
To compare the outcomes as regard: Patient-reported cure rates, Patient satisfaction, Impact on Quality of life (QoL) and sexual function at 3 month & 1 -year follow-up. The objective cure rates will be assessed at 3 month follow-up.
Design:
A pilot prospective randomised study within participating urogynaecology units of the "Scottish Pelvic Floor Network".
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Female Stress Incontinence
Keywords
urodynamic urinary incontinence, sub-urethral tape
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
137 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Single-incision Mini-slings (SIMS- Ajust)
Arm Type
Experimental
Arm Description
AjustTM has polypropylene fixing anchors (one is fixed and the other adjustable) which are anchored onto the obturator membrane. The pulley like system enables adjustment of the tension once the arms have been anchored. Once in place, the anchors rest at right angles to insertion which is claimed to reduce the chances of anchor dislodgment
Arm Title
standared med urethral sling (SMUS)
Arm Type
Other
Arm Description
standard med urethral sling (SMUS)TVT-O, was done as originally described by Deleval et al.
Intervention Type
Procedure
Intervention Name(s)
sub-urethral tape (TVT-O)
Intervention Description
Tension free vaginal tape vs. single incision sub-urethral tension free vaginal tape
Intervention Type
Other
Intervention Name(s)
stand standard mid-urethral sling (TVT-O)
Primary Outcome Measure Information:
Title
• Feasibility of the single incision sub-urethral tape to be done under local anaesthesia
Description
Feasibility of the single incision sub-urethral tape to be done under local anaesthesia?
Number of women approached and declining LA o Number of women in LA group converted to GA
Time Frame
1 year
Secondary Outcome Measure Information:
Title
• Patient-reported Success rates
Description
Patient-reported Success rates
o Assessed by PGI-I "Very Much Improved/ Much Improved."
Time Frame
1 year
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
USI
Mixed incontinence symptoms with predominantly bothering stress component (No DO on UDS).
Primary Incontinence Surgery.
BMI < 35
Ability to understand the information leaflet and sign an informed consent form in English.
All would have had failed or declined PFMT.
Exclusion Criteria:
Mixed incontinence with pre-dominant OAB and/or Neurological conditions e.g. MS.
Detrusor Overactivity on Urodynamics.
Inability to understand English.
Un-willing for randomisation.
Concomitant surgery.
Patient requiring postoperative hospital-stay for medical or social reasons
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohamed Abdel-Fattah, MRCOG
Organizational Affiliation
University of Aberdeen
Official's Role
Principal Investigator
Facility Information:
Facility Name
(Grampian) Aberdeen Royal Infermary
City
Aberdeen
State/Province
Aberdeenshire
ZIP/Postal Code
AB25 2ZD
Country
United Kingdom
12. IPD Sharing Statement
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Feasibility of Comparing Two Surgical Treatment of Female Urodynamic Stress
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