Evaluation of Wear Experience With One Week Reusable Contact Lenses in Habitual Two Week Reusable Lens Wearers

This open-label study is of current Acuvue® Oasys® wearers (2 - week replacement, reusable lenses) who are satisfied with their current lenses. Subjects will be refit into one week reusable contact lenses and will wear lenses for approximately 2 weeks. Subjects will return for vision and lens fit assessments and will complete surveys about their wear experience.

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Key information

Conditions

Myopia Eye Diseases Refractive Errors

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Ohio State University College of Optometry

Columbus, Ohio, 43210, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

At least 18 years of age
Ability to give informed consent
Current Acuvue® Oasys® spherical lens wearer.
Distance visual acuity of 20/25 or better with current contact lenses in each eye.
Good general health defined by, medication use that has not changed within the last 30 days and the absence of medical conditions or treatments that are deemed confounding to the data as determined by the Investigator.
Willing to spend time for the study, which includes: attend three study visits and wear contact lenses on days between study visits.

Exclusion criteria

Current or active ocular inflammation or infection as determined by the Investigator.
Currently pregnant or lactating. (Participants will be asked to self-report these conditions).
Systemic inflammatory disease (i.e. Diabetes, etc.) that could confound study results in the opinion of the investigator.

Treatment and study plan

Biweekly replacement contact lenses

Device

Biweekly replacement reusable contact lenses.

One week replacement contact lenses

Device

One week replacement reusable contact lenses.

Primary outcomes

Subjective Assessment of Lens Wear Experience

Time frame: After 2 weeks of wear in the 1-week replacement reusable lenses.

Subjective assessment of lens wear experience using a CLDEQ-8 survey (contact lens dry eye questionnaire). There are 8 questions about about the presence and intensity of symptoms when wearing contact lenses. When totaling the scores for each question, the lowest possible score=1 and the highest possible score=37. Higher scores result from more prevalent and intense symptoms.

Sponsors and collaborators

Lead sponsor

Ohio State University

Other

Registry information

Official study title

Evaluation of Wear Experience With PRECISION7® Contact Lenses in Habitual Acuvue® Oasys® Lens Wearers

Important dates

Study start: 2024
Primary completion: 2024
Study completion: 2024
First posted: Apr 24, 2024
Registry last updated: Oct 20, 2025

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.

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Completed