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OpenTrials
Completed

NCT Number: NCT03778190

Magnet for Corneal Foreign Bodies

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kendall Regional Medical Center

Miami, Florida, 33175, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

Corneal Foreign Body Removal

Procedure

An eye magnet will be brought close to the foreign body on the surface of the eye in an attempt to remove the foreign body.

Primary outcomes

  1. Success Rate

    Time frame: 5 minutes.

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

Secondary outcomes

  1. Epithelial Damage

    Time frame: 5 minutes

    The percentage of patients in whom the amount of fluorescein uptake on exam was more after the procedure compared to before the procedure.

Sponsors and collaborators

Lead sponsor

Kendall Healthcare Group, Ltd.

Industry

Collaborators

  • Nova Southeastern University

Registry information

Official study title

The Use of a Magnet to Remove Corneal Foreign Bodies

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Dec 19, 2018
Registry last updated
Aug 26, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.