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临床试验/NCT01699425
NCT01699425已完成不适用

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

Hospital Universitari Vall d'Hebron Research Institute6 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2013年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
6
主要终点
Comparison of the cure rates between the single incision sling Ajust and classical transobturator tapes.

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Stress urinary incontinence with urethral hypermobility.

排除标准

  • 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.

结局指标

主要结局

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

时间窗: 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.

次要结局

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

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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