跳至主要内容
临床试验/NCT02502084
NCT02502084已完成不适用

Safety and Effectiveness Evaluation of the Sinusway Device for Endoscopy of the Nasal Cavity and Paranasal Sinuses

3NT Medical Ltd.3 个研究点 分布在 2 个国家目标入组 17 人开始时间: 2015年8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
发起方
入组人数
17
试验地点
3
主要终点
Safety assessed by unanticipated device-related adverse events

研究概览

简要总结

3NT flexible endoscope is a single-use disposable handheld endoscope that provides a means to visualize the nasal cavity and paranasal sinus space and deliver irrigation to treat the sinus ostia and spaces within the paranasal sinus cavities for diagnostic and therapeutic procedures.

详细描述

The rationale behind this feasibility study is to show that accessing and visualization of the nasal anatomy and paranasal sinuses (Maxillary, Frontal and Sphenoid sinuses) in patients suffering from symptoms attributable to sinusitis is feasible; This is an essential step in the development of a system that will later allow visualization, sampling, and treatment of the sinuses via the natural sinus ostium during the patient's first office visit in a minimally invasive manner while enabling treatment by lavage, and minimizing radiation exposure, antibiotic use, multiple office visits, and cost.

研究设计

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

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female patient indicated for primary FESS procedure by the ear, nose and throat (ENT) specialist
  • Patient age: adult (>18 years old)
  • Patients in general good health in the opinion of the investigator as determined by medical history physical examination
  • A patient who is able to understand the requirements of the study, is willing to comply with its instructions and schedules, and agrees to sign the informed consent

排除标准

  • A patient with nasal polyposis
  • A patient indicated for tumor excision
  • Known history of any significant medical disorder, which in the investigator's judgment contraindicates the patient's participation
  • Patients with known current or previous bleeding disorder receiving anticoagulants (e.g., chronic Coumadin treatment)
  • Pregnancy
  • Patients with previous FESS surgery

研究组 & 干预措施

3NT flexible endoscope

Experimental

Evaluation of 3NT flexible endoscope in terms of access and evaluation of the nasal anatomy

干预措施: 3NT flexible endoscope (Device)

结局指标

主要结局

Safety assessed by unanticipated device-related adverse events

时间窗: During hospital stay, up to 1 day

次要结局

  • Performance assessed by anatomical landmarks reached and visualized will be recorded(During procedure, up to 3 hours)

研究者

发起方
3NT Medical Ltd.
申办方类型
Industry
责任方
Sponsor

研究点 (3)

Loading locations...

相似试验