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Safety of Overnight Corneal Reshaping Lenses

Postmarket Study of the Safety of Overnight Corneal Reshaping Lenses

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01272271
Enrollment
1317
Registered
2011-01-07
Start date
2008-02-29
Completion date
2010-10-31
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Keratitis, Myopia

Keywords

Contact lens, Infection, Cornea

Brief summary

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

Interventions

None listed

Sponsors

Bausch & Lomb Incorporated
CollaboratorINDUSTRY
CooperVision, Inc.
CollaboratorINDUSTRY
Ohio State University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
5 Years to 69 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients completing at least 3 months of wearing corneal reshaping lenses

Exclusion criteria

* Less than 3 months of wearing corneal reshaping lenses

Design outcomes

Primary

MeasureTime frameDescription
Microbial keratitis incidence1 yearIncidence of microbial keratitis in children vs. adults with the use of two brands of corneal reshaping lenses.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026