Acuvue Oaysis Contact Lens Wearers Being Refit Into P7 Contact Lenses
NCT ID: NCT06955403
Last Updated: 2025-11-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
40 participants
INTERVENTIONAL
2025-04-15
2025-11-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluation of Wear Experience With One Week Reusable Contact Lenses in Habitual Two Week Reusable Lens Wearers
NCT06382064
Evaluation of ACUVUE® OASYS 1-Day for Astigmatism Contact Lenses With Alternative Lidstock
NCT05713552
Performance Evaluation of Contact Lenses Among a Population of Adapted Contact Lens Wearers
NCT00985231
Accommodative Relief for Uncomfortable Non-Presbyopes
NCT03544216
Evaluation of Approved Contact Lenses
NCT07174596
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
PRECISION7
Determine the likelihood of successfully refitting a satisfied Acuvue Oaysis Contact Lens wearers into P7A CLs.
Precision 7 contact lenses
Acuvue Oaysis contact lens wearers have will be refit into precision 7 contact lenses.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Precision 7 contact lenses
Acuvue Oaysis contact lens wearers have will be refit into precision 7 contact lenses.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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 Criteria
* 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
18 Years
40 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Eminent Ophthalmic Services
UNKNOWN
Southern College of Optometry
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Chris Lievens
Role: PRINCIPAL_INVESTIGATOR
The Southern College of Optometry
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
The Southern College of Optometry
Memphis, Tennessee, United States
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
P7
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.