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Clinical Trials/NCT01699425
NCT01699425
Completed
Not Applicable

Multicentric Comparative Randomized Study of the Single-incision Sling Ajust® Versus Suburethral Transobturator Slings.

Hospital Universitari Vall d'Hebron Research Institute5 sites in 1 country60 target enrollmentMarch 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Female Stress Urinary Incontinence
Sponsor
Hospital Universitari Vall d'Hebron Research Institute
Enrollment
60
Locations
5
Primary Endpoint
Comparison of the cure rates between the single incision sling Ajust and classical transobturator tapes.
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The transobturator tension-free vaginal tape (TOT) procedure has demonstrated high cure rates comparable to those obtained by retropubic suburethral tape, becoming the first line treatment for stress urinary incontinence (SUI) in many cases. The TOT procedure is not exempt from complications such as bleeding, bladder injuries and pain in the thigh/groin. In addition it is commonly performed under general or regional anesthesia1-3. The single-incision mini-slings (SIMS) were developed to reduce the risk of complications by avoiding the blind passage of the trocars through the obturator space. In addition, the use of SIMS could enable surgeons to perform the procedure truly under local anesthesia.

Different devices for SIMS procedure are available. However, the evidence about their efficacy is controversial4-7. The main limitation of these devices could be the predetermined length of the mesh and the weakness on its fixation. The design of the SIMS Ajust® allows adjusting the length of the sling to each individual woman and provides a robust fixation into the obturator membrane. Recent prospective studies on the efficacy and safety of the sling Ajust® have obtained promising results8,9. Even so, the NICE guidelines advise to use SIMS in the context of research studies10.

The objective of this study is to establish if the effectiveness of the SIMS Ajust® is non-inferior to that of a standard TOT, as well as to compare the comorbidity of both procedures. Owing to the new appearance and fast evolution of these procedures, randomized comparative studies with SIMS are required in order to determine its place in the treatment of SUI.

Registry
clinicaltrials.gov
Start Date
March 2013
End Date
May 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Stress urinary incontinence with urethral hypermobility.

Exclusion Criteria

  • Incapacity to understand the information or give their consent.
  • Previous anti-incontinence surgery with slings.
  • Urethral hypomobility (Q-tip test \<30º).
  • Low pressure urethra (MUCP \< 20cmH2O).
  • Detrusor overactivity.

Outcomes

Primary Outcomes

Comparison of the cure rates between the single incision sling Ajust and classical transobturator tapes.

Time Frame: Up to one year

Percentage of patients who are regarded as cured or improved based on the following criteria: * Improvement on the International consultation on Incontinence Urinary Questionnaire-Short Form 1 year after the surgery. * Negative Cough Stress test 1 year after surgery.

Secondary Outcomes

  • Number of participants with adverse events(0, 1, 6 and 12 months after surgery)

Study Sites (5)

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