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Recruiting

NCT Number: NCT06955403

Acuvue Oaysis Contact Lens Wearers Being Refit Into P7 Contact Lenses

Determine the likelihood of successfully refitting a satisfied AOA CL wearers into P7A CLs

Recruiting

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Southern College of Optometry

Memphis, Tennessee, 38104, United States

Location status: Recruiting

Location contact

Chris Lievens, OD

CONTACT

[email protected]

9014815699

About this study

PRECISION7m for Astigmatism is a 1-week, silicone hydrogel (serafilcon A), daily wear, contact lens (CL) with extended wear approval made of a novel material that incorporates the Activ-Flo System. The Activ-Flo System has a moisturizing agent within the CL matrix, which allows for continual release of the moisturizing agents while also providing up to 16 hours of comfortable wear and precise vision for the life of the CL. While initial P7A data are promising, the literature currently lacks a targeted study aimed at determining how patients perform in P7A after transitioning out of other commonly prescribed silicone hydrogel CLs. This transition could be particularly important for patients who have astigmatism given that they tend to struggle with CLs more than spherical CL wearers.1 Thus, the purpose of this study is to determine the success rate of refitting current, satisfied ACUVUE OASYS for Astigmatism CL wearers into P7A. Understanding how a P7A CL wearer reacts to transitioning into P7A from AOA will provide valuable information to partitioners for patient educational purposes, and it will provide credence for refitting successful AOA patients into the newer P7A technology, which could help grow the P7A CL market by not limiting P7A refits to problem-solving events.

Who can participate

Healthy volunteers accepted: Yes

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

  • Inclusion Criteria: Adults, 18- to 40-year-old, AOA CL wearers with best-corrected 20/20 visual acuity or better.
  • 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 Criteria:
  • - 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

Treatment and study plan

Precision 7 contact lenses

Device

Acuvue Oaysis contact lens wearers have will be refit into precision 7 contact lenses.

Primary outcomes

  1. Likert questionnaire

    Time frame: 1 week

    • Likelihood of continuing to wear P7A, 2. Overall satisfaction while wearing P7A, 3. Overall vision while wearing P7A, 4. End of day comfort while wearing P7A, 5. End of day vision while wearing P7A, 6. Overall comfort while wearing P7A, 7. Ability to play sports and perform fitness actives while wearing P7A, 8. Ability to use digital devices while wearing P7A (questions attached). 9. Would recommend the study CLs to a friend.

Study contacts

Contact information is provided by the study sponsor or research team.

Chris Lievens, OD

CONTACT

[email protected]

9014815699

Sponsors and collaborators

Lead sponsor

Southern College of Optometry

Other

Collaborators

  • Eminent Ophthalmic Services

Registry information

Official study title

How Does PRECISION7® for Astigmatism Perform in Current and Successful Acuvue® Oasys for Astigmatism Wearers?

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
May 2, 2025
Registry last updated
Nov 26, 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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