跳至主要内容
临床试验/NCT01611246
NCT01611246已完成不适用

Performance of the Acclarent Iontophoresis System With Earset (IPSES) in Healthy Volunteers

Integra LifeSciences Corporation1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2012年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
22
试验地点
1
主要终点
Number of subjects anesthetized as assessed by Wong-Baker scale

研究概览

简要总结

The study will recruit healthy volunteers to undergo the Iontophoresis procedure using the Acclarent Iontophoresis System with Earset (IPSES).

研究设计

研究类型
Observational

入排标准

年龄范围
12 Months 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • At least 12 months old

排除标准

  • Pregnant or lactating females
  • Subjects with history of sensitivity or reaction to lidocaine, tetracaine, epinephrine, or any hypersensitivity to local anesthetics of the amide type, or any component of the drug solution
  • Significantly atrophic or perforated tympanic membrane
  • Otitis externa
  • Damaged or denuded skin in the auditory canal
  • Electrically sensitive subjects and subjects with electrically sensitive support systems (pacemakers, defibrillators, etc.)
  • Cerumen impaction resulting in a significant amount of cleaning required to visualize the tympanic membrane
  • Evidence of Otitis Media at day of procedure, or within the past three (3) months prior to procedure.

结局指标

主要结局

Number of subjects anesthetized as assessed by Wong-Baker scale

时间窗: Day 1

次要结局

  • Number of participants with serious adverse events(Day 1)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验