RecruitingNot ApplicableNCT06955403
Acuvue Oaysis Contact Lens Wearers Being Refit Into P7 Contact Lenses
How Does PRECISION7® for Astigmatism Perform in Current and Successful Acuvue® Oasys for Astigmatism Wearers?
Sponsor
Southern College of Optometry
Enrollment
40 participants
Start Date
Apr 15, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
Determine the likelihood of successfully refitting a satisfied AOA CL wearers into P7A CLs
Eligibility
Min Age: 18 YearsMax Age: 40 Years
Inclusion Criteria8
- Participants will be required to have worn AOA CLs for at least 3 months in the past year and currently wearing these CLs.
- All participants will be required to have a CLDEQ-8 score <12 while wearing their habitual CLs (AOA CLs) and to indicate that they are satisfied with AOA CLs (Yes/No).
- Participants will be required to be able to wear P7A CLs (astigmatism ≥0.75D OD/OS).
- Astigmatism ranging from 0.75 D to 2.50 D in each eye
- Participants will be required to wear the study CLs for ≥13 hours with no overnight wear
- Participants will be willing to wear the CL every day of the week, except during the washout period
- Participants will be required to provide a glasses prescription that is less than 3 years old
- \-
Exclusion Criteria12
- \- Have presbyopia and/or need a reading add as determined during their initial manifest refraction
- Have worn P7A in the past
- Are past rigid CL wearers
- Have a history of being diagnosed with dry eye or ocular allergies
- Have known systemic health conditions that are thought to alter tear film physiology
- Have a history of viral eye disease
- Have a history of ocular surgery
- Have a history of severe ocular trauma
- Have a history of corneal dystrophies or degenerations
- Have active ocular infection or inflammation
- Are currently using isotretinoin-derivatives or ocular medications
- Are pregnant or breast feeding
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Interventions
DEVICEPrecision 7 contact lenses
Acuvue Oaysis contact lens wearers have will be refit into precision 7 contact lenses.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06955403