Safety of Overnight Corneal Reshaping Lenses

This retrospective chart review study compares the incidence of corneal inflammation due to infection in children vs. adult patients wearing overnight corneal reshaping lenses.

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Key information

Conditions

Keratitis Corneal Diseases Eye Diseases Infections Myopia Refractive Errors

Age range

5 year–69 year

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

Patients completing at least 3 months of wearing corneal reshaping lenses

Exclusion criteria

Less than 3 months of wearing corneal reshaping lenses

Treatment and study plan

Primary outcomes

Microbial keratitis incidence

Time frame: 1 year

Incidence of microbial keratitis in children vs. adults with the use of two brands of corneal reshaping lenses.

Sponsors and collaborators

Lead sponsor

Ohio State University

Other

Collaborators

Bausch & Lomb Incorporated
CooperVision, Inc.

Registry information

Official study title

Postmarket Study of the Safety of Overnight Corneal Reshaping Lenses

Important dates

Study start: 2008
Primary completion: 2010
Study completion: 2010
First posted: Jan 7, 2011
Registry last updated: Apr 29, 2024

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.

Published trials that share one or more normalized conditions with this study.

Completed