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临床试验/NCT04173130
NCT04173130已完成不适用

Étude Monocentrique de faisabilité d'un Nouveau Dispositif Pour le Traitement de la Fissure Anale Par Toxine Botulique (FR) Monocentric Feasibility Study for a New Medical Device for the Treatment of Anal Fissure With Botulinum Toxin (EN)

Dieter Hahnloser2 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2019年11月11日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
4
试验地点
2
主要终点
Feasibility of the injection of the botulin toxin with the device under investigation

研究概览

简要总结

Monocentric feasibility study for a new device for the treatment of anal fissure with botulinum toxin.

详细描述

Anal fissure is a common anal disease. This is a longitudinal tear in the distal part of the anal canal. The fissure provokes a spasm of the internal anal sphincter and as such pain and eventually bleeding.

There are currently 3 different treatments. All available treatments tend to relax the anal sphincter, which reduces pain and promotes fissure healing.

The first treatment consists in the local application of cream into the anal canal.

The second option is the injection of botulinum toxin into the internal or external anal sphincter. Finally the third option is a surgical intervention, most frequently a lateral sphincterotomy.

Although the usefulness of botulinum toxin to treat anal fissure has been demonstrated, the results vary. This is most likely largely due to the fact that there is no standardized way to inject botulinum toxin and that there is a significant learning curve. In addition, the gesture is not without risk for the operator.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Device Feasibility
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • adult patients suffering from anal fissures for a minimum of 6 weeks.
  • informed consent signed

排除标准

  • Contraindication to the use of botulinum toxin or any known allergies
  • Pregnant or breastfeeding women
  • Immune deficiency, immunosuppression
  • Anticoagulant treatment
  • Previous pelvic radiotherapy
  • Acute anal inflammation (eg.proctitis)
  • Internal hemorrhoids of grade 2 or higher
  • Anal fissure that did not respond to a previous treatment by botulinum toxin
  • History of lateral sphincterotomy
  • Cardiopulmonary disease leading to reduced function of the Cardiopulmonary system

结局指标

主要结局

Feasibility of the injection of the botulin toxin with the device under investigation

时间窗: This outcome will be assessed right after the use of the device under investigation, at day 1 (day of the intervention).

The operator shall answer by yes or no. If yes, the procedure is further assessed (see outcome 2)

次要结局

  • Safety of the procedure by assessing adverse events, device deficiencies and identifying new risks(day 1, day +7, day +56)
  • Assessment of the relaxation of the internal anal sphincter(day 1, day +7, day +56)
  • Assessment of the patient's tolerance: visual analogic scale (VAS)(This outcome will be assessed right after the use of the device under investigation, at day 1 (day of the intervention).)
  • Assessment of the healing rate(day 1, day +56)
  • Assessment of the procedure by the operator(This outcome will be assessed right after the use of the device under investigation, at day 1 (day of the intervention).)
  • Assessment of the incontinence(day 1, day +7, day +56)

研究者

发起方
Dieter Hahnloser
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Dieter Hahnloser

Professor

University of Lausanne Hospitals

研究点 (2)

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