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临床试验/NCT04743817
NCT04743817已完成不适用

Feasibility Evaluation of the OtoSet - Ear Cleaning System

SafKan4 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2021年3月31日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
SafKan
入组人数
110
试验地点
4
主要终点
Safety as Assessed by Adverse Events

研究概览

简要总结

This is a single center study. 100 ears are planned (up to 100 patients). Each subject will have one or both ears cleaned with OtoSet. The subject's level of earwax will be evaluated before and after by an evaluator.

详细描述

This is a single center study. 100 ears are planned (up to 100 patients). Each subject will have one or both ears cleaned with OtoSet. The subject's level of earwax will be evaluated before and after by an evaluator.

Screening data will be reviewed to determine subject eligibility. Subjects who meet all inclusion criteria and none of the exclusion criteria will be entered into the study.

Total duration of subject participation will be 1 day with a follow up call within 2-4 days after the procedure. Total duration of the study is expected to be 3 months.

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

入选标准

  • Mild (1), Moderate (2), or Complete (3) occlusion of the ear canal based on the Degree of Occlusion Scale in one or both ears
  • Informed consent obtained from subject or subject's legal representative and ability for subject to comply with the requirements of the study

排除标准

  • Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient of the quality of data
  • Subject has life threatening illness
  • Subject has immune deficiency

结局指标

主要结局

Safety as Assessed by Adverse Events

时间窗: Treatment Visit (Day 1) through follow-up call (Day 2-4)

Incidence of adverse events with severity defined using the National Cancer Institute's Common Terminology Criteria for Adverse Events (4 point scale) (1 = mild; 4 = life-threatening)

Efficacy as Assessed by Occlusion Scale

时间窗: Treatment Visit (Day 1) (pre- to post-procedure)

Improvement of 1.0 on the Degree of Occlusion Scale (4 point scale) pre- and post-procedure evaluation (score 0 = no occlusion; 3 = complete occlusion)

次要结局

未报告次要终点

研究者

发起方
SafKan
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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