Evaluation of Wear Experience With Daily Contact Lenses

The Ohio State University

Status: Completed

Conditions: Contact Lens

Treatments: Device: Precision1® Daily Disposable Contact Lens

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT05096156

2021H0118

Details and patient eligibility

About

To evaluate the wear experience of current monthly replacement contact lens wearers after they have been fit into a daily disposable contact lens.

Enrollment: 30 patients

Sex: All

Ages: 18 to 40 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Currently wear Biofinity® monthly replacement spherical contact lenses.
• Distance visual acuity of 20/25 or better with current contact lenses.
• Good general health (defined by medication use that has not changed within the last month and the absence of medical conditions or treatments that are deemed confounding to the data as determined by the PI).
• Ability to give informed consent.
• Willing to spend time for the study, which includes attending two study visits and wearing contact lenses on days between study visits.

Exclusion criteria

• No current ocular inflammation or infection.
• Not currently pregnant or lactating.

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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30 participants in 1 patient group

All participants are fit with the study daily disposable lenses

Experimental group

Description:

All subjects are re-fit into their habitual monthly replacement contact lenses. Subjects are requested to wear the lenses for one week, for a minimum of at least 6 hours per day for 5 days. Upon return, subjects are refit into the daily disposable contact lenses.

Treatment:

Device: Precision1® Daily Disposable Contact Lens