NCT Number: NCT01699425
Multicentric Comparative Randomized Study of the Single-incision Sling Ajust® Versus Suburethral Transobturator Slings.
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.
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Notify MeKey information
Conditions
Age range
18 year–90 year
Sex eligibility
Female
Study type
Interventional
Phase
Not applicable
Primary location
Hospital Universitari Vall d'Hebron, Barcelona, Spain
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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.
Treatment and study plan
Classical transobturator sling
DeviceControl group
Other names: Align®
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
Time frame: 0, 1, 6 and 12 months after surgery
Comparison of the intra- and postoperative complications between procedures
Other outcomes
-
Change in the Maximal Urethral Closure Pressure.
Time frame: One year after surgery.
Comparison of the changes in the Maximal Urethral Closure Pressure (cmH2O) measured preoperatively and 1 year after surgery.
Sponsors and collaborators
Lead sponsor
Hospital Universitari Vall d'Hebron Research Institute
Other
Collaborators
- Hospital Universitari de Bellvitge
- Hospital de Viladecans
- Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta
- Serveis de Salut Integrats Baix Empordà
Registry information
Important dates
- Study start
- 2013
- Primary completion
- 2016
- Study completion
- 2016
- First posted
- Oct 3, 2012
- Registry last updated
- Mar 28, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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