跳至主要内容
临床试验/NCT00210444
NCT00210444已完成2 期

A Phase II, Multicentre, Open, Randomised, Parallel Group, Dose Ranging Study to Define the Efficacy of Dysport® in the Treatment of Anal Fissure.

Ipsen14 个研究点 分布在 4 个国家目标入组 168 人开始时间: 2003年6月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
Ipsen
入组人数
168
试验地点
14
主要终点
Healing of the anal fissure by complete re-epithelisation of the anal canal mucosa.

研究概览

简要总结

To evaluate the effect on healing rates of two different prognostic factors in patients treated with Dysport® for anal fissure: duration of fissure and dose of study drug

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
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

  • Patients having idiopathic anal fissure in the posterior anal midline
  • Patients having anal fissure present for less than 6 months
  • Patients having symptoms (pain) present for a minimum of 2 weeks and not responding after 2 weeks of standard therapy (diet, laxatives, sitz-bathes)

排除标准

  • Patients having anal fistulas or anal fissure of various causes such as Crohn disease, Behcet infectious ulceration, anal suppuration, subfissural infiltration, abscesses, acute haemorrhoidal attacks or inflammatory bowel disease
  • Patients having idiopathic anal fissure in the anterior anal midline
  • Patients having lateral or multiple fissures
  • Patients having anal or perianal cancer
  • Patients who underwent previous anal surgery or have cicatricial alterations or post-surgical cicatricial lesions
  • Patients receiving drugs affecting neuromuscular transmission
  • Patients who have received topical anaesthetic within 3 days of injection
  • Patients receiving local treatment by myorelaxing agent
  • Patients receiving prohibited analgesics
  • Patients having bleeding disturbances or currently using coumarin derivates
  • Patients having myasthenia or any genetic muscle disease

结局指标

主要结局

Healing of the anal fissure by complete re-epithelisation of the anal canal mucosa.

次要结局

  • Improvement of anal pain measured by the patients on Analogue Visual Pain Scale.

研究者

发起方
Ipsen
申办方类型
Industry
责任方
Sponsor

研究点 (14)

Loading locations...

相似试验

Efficacy Study of Dysport® in the Treatment of Anal... | 临床试验