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临床试验/NCT03778190
NCT03778190已完成不适用

The Use of a Magnet to Remove Corneal Foreign Bodies

Kendall Healthcare Group, Ltd.2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2018年12月4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
10
试验地点
2
主要终点
Success Rate

研究概览

简要总结

This is a prospective, interventional study to assess the effectiveness and safety of a commercially available "eye magnet" to remove corneal foreign bodies.

详细描述

The vast majority of corneal foreign bodies are metallic and thus are frequently ferromagnetic. Consequently, it may be possible to use a magnet to remove most corneal foreign bodies. There are commercially available products for removing corneal foreign bodies, but there are no published studies assessing these devices.

This will be a prospective interventional study to assess the use of an eye magnet for the removal of metallic corneal foreign bodies in the emergency department.

After the patient signs written, informed consent, the physician will attempt to remove the corneal foreign body with the North by Honeywell 326734G Eye Magnet with Loop. If the physician is unable to remove the corneal foreign body with the magnet, he or she may proceed with standard care.

The treating physician will fill out a brief data collection form for each patient to track various outcomes as discussed below.

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

  • present to the emergency department with a metallic corneal foreign body

排除标准

  • prisoners
  • pregnant women
  • have pacemakers or metallic facial implants
  • possible globe rupture

结局指标

主要结局

Success Rate

时间窗: 5 minutes.

The percentage of patients in whom the magnet successfully removed the foreign body.

次要结局

  • Epithelial Damage(5 minutes)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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