跳至主要内容
临床试验/DRKS00027395
DRKS00027395招募中不适用

Monitoring of the safety and the performance of the Endoscopic Cap electrode (ECE50)

MED-EL Elektromedizinische Geräte GmbH0 个研究点目标入组 100 人开始时间: 2021年12月21日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • Legal adults (i.e., as a general rule patients = 18 years old)
  • Legal adults requiring a diagnosis for a disorder that could be traced back to uni- or bilateral dysfunction of one or more laryngeal muscle(s) of the posterior cricoid region
  • Signed and dated informed consent before the start of any registry-specific procedure for all the recruited subjects

排除标准

  • Lack of compliance with any inclusion criteria
  • Use of an active medical implant
  • Known allergies or intolerance to the material used for this registry
  • Parallel participation in a device/drug registry in the period of data collection, which could confound the results of the registry
  • Anything that, in the opinion of the Registry Responsible, would place the subject at increased risk or preclude the subject's full compliance with the general requirements of this registry

研究者

发起方
MED-EL Elektromedizinische Geräte GmbH

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