N/A N=10 Treatment

Magnet for Corneal Foreign Bodies

Corneal Foreign Body

Bottom Line

View on ClinicalTrials.gov: NCT03778190 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Aug 2020

Primary outcome: Primary: Success Rate — 1 Participants

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Corneal Foreign Body Removal (Procedure)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: Kendall Healthcare Group, Ltd.
Primary completion: Nov 2019

Outcome Measures

Outcome	Result	p-value
PRIMARY Success Rate	1	—
SECONDARY Epithelial Damage	—	—

Summary

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

Eligibility Criteria

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

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03778190). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.