Efficacy of Sacral Nerve Stimulation Before Definitive Implantation (SNStest)
Efficacy of Sacral Nerve Stimulation Before Definitive Implantation: a Multicenter Randomized, Double Blind, Crossover Trial
研究概览
详细说明
Sacral nerve stimulation (SNS) is an emerging treatment for patients with severe faecal incontinence when conservative measures fail and surgical repair is not indicated. In a minimally-invasive approach and under local anaesthesia, an electrode is placed around sacral nerve root S2-4 and electrical stimulation is applied to the sacral spinal nerves. Effectiveness of SNS is definitively not only explained by placebo effect but the pathophysiologic mechanisms remain unclear. Suggested pathways include modulation of afferent nerve fibres and direct stimulation of the pelvic floor and anal sphincter muscle. After placement of the electrode, the patient is stimulated by an external stimulator for 1-3 weeks. During this period, the patient documents the number of faecal incontinence episodes or urgencies in a symptom diary. By convention, indication for permanent stimulation is based on a 50% reduction in the number of episodes. After a successful testing period, the permanent stimulator is implanted, generally in the upper gluteal region.
Previous studies report success rates up to 80%. The only randomized trial with a proper sample size evaluated the efficacy of SNS after definite implantation. In this study, 63% of the patients felt improved during the placebo period and might not really benefit from the device. The real success rate of SNS is therefore likely to be considerably lower. Efficacy of SNS during the testing phase has never been assessed in a blinded randomized study.
研究类型
阶段
- 不适用
联系人和位置
学习地点
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Vaud
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Lausanne、Vaud、瑞士、1005
- Visceral surgery, university hospital
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参与标准
资格标准
适合学习的年龄
- 孩子
- 成人
- 年长者
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- All patients admitted to SNS test for treatment of faecal incontinence after unsuccessful conservative (or surgical) treatment.
Exclusion criteria:
- Absence of informed consent.
- Patients not speaking french or german.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:交叉作业
- 屏蔽:三倍
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:A: sacral first
Phase 1: sacral nerve stimulation crossover Phase 2 : sham stimulation
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sacral nerve stimulation for fecal incontinence
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实验性的:B: sham first
Phase 1: sham stimulation crossover Phase 2: sacral nerve stimulation
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sacral nerve stimulation for fecal incontinence
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Primary success rate of SNS after 7 days. By convention this is assessed by >50% reduction in the number of episodes in the symptom diary.
大体时间:24 months
|
24 months
|
合作者和调查者
调查人员
- 首席研究员:Martin Hubner, MD、Visceral Surgery, University Lausanne, Switzerland
- 研究主任:Jean-Claude Givel, Professor、Visceral Surgery, University Lausanne, Switzerland
- 学习椅:Nicolas Demartines, Professor、Visceral Surgery, University Lausanne, Switzerland
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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