NL-OMON42228已完成不适用
An early clinical feasibility study of a new prosthesis: the NewBreez® Intralaryngeal device; a possible solution for severe aspiration in head and neck cancer patients - An intralaryngeal device for a dysfunctional larynx
Antoni van Leeuwenhoek Ziekenhuis0 个研究点目标入组 5 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
- 5
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
- •- Patients who have been treated successfully for HNC and are free of disease minimally one year after treatment; and
- •- Patients with difficulties in feeding and/or breathing due to a dysfunctional larynx, necessitating prolonged (> 6 months) use of a (nasogastric or percutaneous) feeding tube and a tracheotomy, which are unlikely to be removed; and
- •- Patients who are motivated to undergo the operation; and
- •- Patients are willing to provide written informed consent prior to participation.
排除标准
- •- Patients under the age of 18 years; or
- •- Patients with clotting disorders; or
- •- Patients with Chronic Obstructive Pulmonary Disease (COPD); or
- •- Patients with recurrent or residual HNC disease; or
- •- Patients with upper esophageal obstruction or stenosis on videofluoroscopy; or
- •- Patients who are unfit to undergo general anaesthesia, as judged by the anaesthetist.
研究者
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