跳至主要内容
临床试验/NL-OMON37173
NL-OMON37173已完成不适用

2-duct ligation versus botulinum toxin for severe drooling in children with cerebral palsy - 2-duct ligation versus botulinum toxin for severe drooling

niversitair Medisch Centrum Sint Radboud0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
2 至 99(—)

入选标准

  • - Age 6 years or above
  • - Cerebral palsy or other non-progressive neurological disease
  • - Severe drooling (Drooling Frequency >=3; Drooling Severity >=2)
  • - Conservative treatment has not led to adequate reduction of droolng
  • - Informed consent
  • - Cognitive ability of parents is adequate to participate in the study, as judged by the researchers.
  • - Participants are motived to return for follow up after 2, 8 and 32 weeks.

排除标准

  • - Concurrent participation in other medical study
  • - Previous surgery or anatomical abnormalities that prohibit either application of botulinum toxin or surgery
  • - Concurrent other treatment for drooling
  • - Use of benzodiazepines
  • - Allergy to botulinum toxin or other contraindication for botulinumtoxin or surgery.

研究者

发起方
niversitair Medisch Centrum Sint Radboud

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