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临床试验/NCT05762497
NCT05762497已完成不适用

Pilot Feasibility Study of a Moldable Peristomal Adhesive for Pulmonary and Speech Rehabilitation After Total Laryngectomy

Fondazione Policlinico Universitario Agostino Gemelli IRCCS1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2022年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
1
主要终点
Investigation about product performance

研究概览

简要总结

Loss of voice is one of the greater consequences of total laryngectomy. The voice prosthesis allows the patients to speak again in a very short time but forces them to use one hand when speaking. In order to reduce this discomfort and to allow "hands-free" speaking, an Automatic Speaking Valve (ASV) has been designed which is positioned on a peristomal adhesive.

Peristomal adhesives, however, tend to detach under the influence of mucus, cough, or phonatory pressure. Consequently, the current regular use of the automatic speaking valve in laryngectomees is very low. As a possible solution, Atos Medical AB has developed a moldable peristomal adhesive made of a thermoplastic elastomer, which becomes transparent and moldable when heated and facilitates precise contouring in situ. As the material cools, it loses its malleability but retains the integrity of the molded shape.

The expectation was that the moldable adhesive would provide a better individual fit and therefore longer fixation (especially when using the ASV).

To study the feasibility of this device, 10 total laryngectomized patients were asked to use the new moldable peristomal adhesive for two weeks in conjunction with their normal daily routine for adhesive application and removal, and speech rehabilitation.

研究设计

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

入排标准

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

入选标准

  • •Have undergone total laryngectomy
  • •Over the age of 18
  • •voice prosthesis user
  • •Experience in the use of adhesive and HMEs
  • •At least 3 months after total laryngectomy
  • •At least 6 months after the end of adjuvant radiotherapy
  • •Signature of the informed consent

排除标准

  • •Medical issues that prevent the use of HMEs and/or adhesives
  • •Recurrent or metastatic active disease
  • •Reduced mobility of the arms and/or hands
  • •Inability to understand the information and/or to provide informed consent
  • •Insufficient cognitive ability to handle HME or moldable adhesive

研究组 & 干预措施

Laryngectomized patients

Experimental

干预措施: Moldable adhesive (Other)

结局指标

主要结局

Investigation about product performance

时间窗: 2 weeks

Adhesive lifetime during hands-free speech use \[hours\]

次要结局

  • Parameters were expected to influence product performance and patient preference(2 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Parrilla Claudio

Principal Investigator

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

研究点 (1)

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