PUG: Evaluating the Performance of Precision1 Daily Disposable Contact Lens in a Group of Heavy Digital Device Users

Sponsor
University of Waterloo (Other)
Overall Status
Completed
CT.gov ID
NCT04201639
Collaborator
Alcon Research (Industry)
35
1
1
21.5
1.6

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the performance of Precision1 DD CLs with regard to subjective symptoms (dryness, comfort, vision), lens fit and time to haze in CL wearers who identify themselves as heavy digital devices users (at least 6 hours of digital device use per day).

Condition or Disease Intervention/Treatment Phase
  • Device: Verofilcon A contact lenses
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
35 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Evaluating the Performance of Precision1 Daily Disposable Contact Lens in a Group of Heavy Digital Device Users
Actual Study Start Date :
Dec 13, 2019
Actual Primary Completion Date :
Sep 27, 2021
Actual Study Completion Date :
Sep 27, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Refit

Refit and dispense patient with Verofilcon A contact lenses and evaluate lens performance.

Device: Verofilcon A contact lenses
Daily disposable silicone hydrogel contact lenses indicated for the optical correction of refractive ametropia (myopia and hyperopia)
Other Names:
  • Precision1™
  • Outcome Measures

    Primary Outcome Measures

    1. Subjective comfort after contact lens insertion [Dispense Visit (Day 0)]

      Participants rate their comfort after insertion on a scale from 0 (worst) to 100 (best).

    2. Subjective dryness after contact lens insertion [Dispense Visit (Day 0)]

      Participants rate their dryness after insertion on a scale from 0 (worst) to 100 (best).

    3. Subjective rating of clarity of vision after contact lens insertion [Dispense Visit (Day 0)]

      Participants rate their clarity of vision after insertion on a scale from 0 (worst) to 100 (best).

    4. Subjective comfort after contact lens insertion [Day 1]

      Participants rate their comfort after insertion on a scale from 0 (worst) to 100 (best).

    5. Subjective dryness after contact lens insertion [Day 1]

      Participants rate their dryness after insertion on a scale from 0 (worst) to 100 (best).

    6. Subjective rating of clarity of vision after contact lens insertion [Day 1]

      Participants rate their clarity of vision after insertion on a scale from 0 (worst) to 100 (best).

    7. Subjective comfort after contact lens insertion [Day 7]

      Participants rate their comfort after insertion on a scale from 0 (worst) to 100 (best).

    8. Subjective dryness after contact lens insertion [Day 7]

      Participants rate their dryness after insertion on a scale from 0 (worst) to 100 (best).

    9. Subjective rating of clarity of vision after contact lens insertion [Day 7]

      Participants rate their clarity of vision after insertion on a scale from 0 (worst) to 100 (best).

    10. Subjective comfort after contact lens insertion [Day 10]

      Participants rate their comfort after insertion on a scale from 0 (worst) to 100 (best).

    11. Subjective dryness after contact lens insertion [Day 10]

      Participants rate their dryness after insertion on a scale from 0 (worst) to 100 (best).

    12. Subjective rating of clarity of vision after contact lens insertion [Day 10]

      Participants rate their clarity of vision after insertion on a scale from 0 (worst) to 100 (best).

    13. Subjective comfort after contact lens insertion [Followup visit (Day 12-16)]

      Participants rate their comfort after insertion on a scale from 0 (worst) to 100 (best).

    14. Subjective dryness after contact lens insertion [Followup visit (Day 12-16)]

      Participants rate their comfort after insertion on a scale from 0 (worst) to 100 (best).

    15. Subjective rating of clarity of vision after contact lens insertion [Followup visit (Day 12-16)]

      Participants rate their comfort after insertion on a scale from 0 (worst) to 100 (best).

    16. Subjective comfort with contact lens wear after 6 hours of digital device use [Dispense Visit (Day 0)]

      Participants rate their comfort after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    17. Subjective dryness with contact lens wear after 6 hours of digital device use [Dispense Visit (Day 0)]

      Participants rate their dryness after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    18. Subjective rating of vision clarity with contact lens wear after 6 hours of digital device use [Dispense Visit (Day 0)]

      Participants rate their vision clarity after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    19. Subjective comfort with contact lens wear after 6 hours of digital device use [Day 1]

      Participants rate their comfort after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    20. Subjective dryness with contact lens wear after 6 hours of digital device use [Day 1]

      Participants rate their dryness after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    21. Subjective rating of vision clarity with contact lens wear after 6 hours of digital device use [Day 1]

      Participants rate their vision clarity after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    22. Subjective comfort with contact lens wear after 6 hours of digital device use [Day 7]

      Participants rate their comfort after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    23. Subjective dryness with contact lens wear after 6 hours of digital device use [Day 7]

      Participants rate their dryness after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    24. Subjective rating of vision clarity with contact lens wear after 6 hours of digital device use [Day 7]

      Participants rate their vision clarity after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    25. Subjective comfort with contact lens wear after 6 hours of digital device use [Day 10]

      Participants rate their comfort after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    26. Subjective dryness with contact lens wear after 6 hours of digital device use [Day 10]

      Participants rate their dryness after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    27. Subjective rating of vision clarity with contact lens wear after 6 hours of digital device use [Day 10]

      Participants rate their vision clarity after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    28. Subjective comfort with contact lens wear after 6 hours of digital device use [Followup visit (Day 12-16)]

      Participants rate their comfort after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    29. Subjective dryness with contact lens wear after 6 hours of digital device use [Followup visit (Day 12-16)]

      Participants rate their dryness after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    30. Subjective rating of vision clarity with contact lens wear after 6 hours of digital device use [Followup visit (Day 12-16)]

      Participants rate their vision clarity after 6 hours of digital device use on a scale from 0 (worst) to 100 (best).

    31. Subjective Comfort at End of Day with contact lens wear [Dispense Visit (Day 0)]

      Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).

    32. Subjective dryness at End of Day with contact lens wear [Dispense Visit (Day 0)]

      Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).

    33. Subjective rating of vision clarity at End of Day with contact lens wear [Dispense Visit (Day 0)]

      Participants rate their end of day vision clarity on a scale from 0 (worst) to 100 (best).

    34. Subjective Comfort at End of Day with contact lens wear [Day 1]

      Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).

    35. Subjective dryness at End of Day with contact lens wear [Day 1]

      Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).

    36. Subjective rating of vision clarity at End of Day with contact lens wear [Day 1]

      Participants rate their end of day vision clarity on a scale from 0 (worst) to 100 (best).

    37. Subjective Comfort at End of Day with contact lens wear [Day 7]

      Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).

    38. Subjective dryness at End of Day with contact lens wear [Day 7]

      Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).

    39. Subjective rating of vision clarity at End of Day with contact lens wear [Day 7]

      Participants rate their end of day rating of vision clarity on a scale from 0 (worst) to 100 (best).

    40. Subjective Comfort at End of Day with contact lens wear [Day 10]

      Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).

    41. Subjective dryness at End of Day with contact lens wear [Day 10]

      Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).

    42. Subjective rating of vision clarity at End of Day with contact lens wear [Day 10]

      Participants rate their end of day vision clarity on a scale from 0 (worst) to 100 (best).

    43. Subjective Comfort at End of Day with contact lens wear [Followup visit (Day 12-16)]

      Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).

    44. Subjective dryness at End of Day with contact lens wear [Followup visit (Day 12-16)]

      Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).

    45. Subjective rating of vision clarity at End of Day with contact lens wear [Followup visit (Day 12-16)]

      Participants rate their end of day rating of vision clarity on a scale from 0 (worst) to 100 (best).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 40 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    1. Is between 18 and 40 years of age (inclusive) and has full legal capacity to volunteer;

    2. Has read and signed an information consent letter;

    3. Is willing and able to follow instructions and maintain the appointment schedule;

    4. Is a heavy digital device user (at least 6 hours on a typical day using any combination of digital devices such as PC, laptop, smartphone, or tablet);

    5. Is a habitual wearer of daily, spherical, soft contact lenses (no bifocal or multifocal contact lenses, no extended wear or monovision, not a current wearer of Precision1 lenses) for at least 5 days/week and at least 10 hours/day during the month prior to enrollment;

    6. Has a vertex corrected spherical equivalent distance refraction that ranges between -0.50D to -6.00D in each eye;

    7. Has a vertex corrected refractive cylinder of no more than -1.00D cylindrical correction in each eye after vertexing to the corneal plane;

    8. Demonstrates an acceptable fit and achieves best corrected visual acuity of at least 0.20 log MAR in each eye with Precision1 contact lenses;

    9. Is willing to wear Precision1 CLs at least 5 days per week and 10 hours per day throughout the study;

    Exclusion Criteria:
    1. Is participating in any concurrent clinical or research study;

    2. Has any known active* ocular disease and/or infection;

    3. Has a systemic condition that in the opinion of the investigator may affect a study outcome variable;

    4. Is using any systemic or topical medications that in the opinion of the investigator may affect a study outcome variable;

    5. Has known sensitivity to the diagnostic pharmaceuticals to be used in the study;

    6. Is pregnant, lactating or planning a pregnancy at the time of enrolment;

    7. Is aphakic;

    8. Has undergone refractive error surgery;

    • For the purposes of this study, active ocular disease is defined as infection or inflammation which requires therapeutic treatment. Mild (i.e. not considered clinically relevant) lid abnormalities (blepharitis, meibomian gland dysfunction, papillae), corneal and conjunctival staining and dry eye are not considered active ocular disease. Neovascularization and corneal scars are the result of previous hypoxia, infection or inflammation and are therefore not active.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Centre for Ocular Research & Education Waterloo Ontario Canada N2L 3G1

    Sponsors and Collaborators

    • University of Waterloo
    • Alcon Research

    Investigators

    • Principal Investigator: Lyndon Jones, PhD, FCOptom, Centre for Ocular Research & Education

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Waterloo
    ClinicalTrials.gov Identifier:
    NCT04201639
    Other Study ID Numbers:
    • 41694
    First Posted:
    Dec 17, 2019
    Last Update Posted:
    Oct 4, 2021
    Last Verified:
    Oct 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Product Manufactured in and Exported from the U.S.:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 4, 2021