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临床试验/NCT01230450
NCT01230450已完成1 期

Feasibility of Comparing Two Surgical Treatment of Female Urodynamic Stress Incontinence (SITOT)

University of Aberdeen1 个研究点 分布在 1 个国家目标入组 137 人开始时间: 2009年11月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
137
试验地点
1
主要终点
• Feasibility of the single incision sub-urethral tape to be done under local anaesthesia

研究概览

简要总结

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).

详细描述

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:

  1. Establish the feasibility of the "Single incision sub-urethral tapes" to be done under local anaesthesia.
  2. The feasibility of randomisation to the standard surgical treatment TVT-O / TVT.
  3. 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,
  4. 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".

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
20 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •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.

排除标准

  • •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

研究组 & 干预措施

Single-incision Mini-slings (SIMS- Ajust)

Experimental

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

干预措施: sub-urethral tape (TVT-O) (Procedure)

standared med urethral sling (SMUS)

Other

standard med urethral sling (SMUS)TVT-O, was done as originally described by Deleval et al.

干预措施: stand standard mid-urethral sling (TVT-O) (Other)

结局指标

主要结局

• Feasibility of the single incision sub-urethral tape to be done under local anaesthesia

时间窗: 1 year

* 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

次要结局

  • • Patient-reported Success rates(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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