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临床试验/NL-OMON50048
NL-OMON50048已完成不适用

The Swallowing Exercise Aid in Total Laryngectomy: Feasibility, Adherence and a Multidimensional Assessment of Functional-, Physical-, and Patient-reported outcomes - SEATTLE

Antoni van Leeuwenhoek Ziekenhuis0 个研究点目标入组 20 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
20

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
18 至 99(—)

入选标准

  • >= 18 years or older
  • Undergone a TLE
  • At least six months post TLE
  • At least six months postoperative (chemo-) radiotherapy (if applicable)
  • Using Tracheoesophageal speech
  • Oral intake of a modified diet (FOIS 2 - 6) or who experience swallowing
  • Signed informed consent

排除标准

  • Unable to understand the patient information
  • Unable to understand the informed consent
  • Unable to comprehend and use the SEA
  • Unable or unwilling to provide informed consent
  • Neuro-degenerative diseases, for instance, dementia, Parkinson, Korsakov

研究者

发起方
Antoni van Leeuwenhoek Ziekenhuis

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