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Customizing Myopia Control With Multifocal Toric Contact Lens

Primary Purpose

Refractive Errors, Myopia

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Intelliwave multifocal, toric, soft contact lens
Intelliwave toric, soft contact lens
Sponsored by
University of Alabama at Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Refractive Errors focused on measuring Myopia, Multifocal contact lens, Refractive error, Myopia treatment, Myopia control, Myopia management

Eligibility Criteria

8 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 8 to 12 years, inclusive, at baseline examination
  • -0.50 to -6.00 D, inclusive, spherical component, cycloplegic autorefraction
  • ≥0.75 DC, cycloplegic autorefraction
  • 0.1 logMAR or better best-corrected visual acuity in each eye

Exclusion Criteria:

  • Eye disease or refractive error conditions (e.g., keratoconus, retinal abnormalities, retinopathy of prematurity, etc.)
  • Ocular surgery, severe ocular trauma, active ocular infection or inflammation
  • Subjects with a condition or in a situation, which in the examiner's opinion, may put the subject at significant risk, may confound the study results, or may significantly interfere with their participation in the study.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    Toric soft contact lens

    Multifocal toric soft contact lens

    Arm Description

    Toric soft contact lens

    A multifocal toric soft contact lens with a +2.00 D add.

    Outcomes

    Primary Outcome Measures

    Refractive error progression
    Refractive error measured by cycloplegic autorefraction in both eyes, will be measured at baseline and at one year to assess the difference in spherical component of the refractive error between the treatment group (multifocal toric soft contact lens) and the control group (toric soft contact lens)
    Axial length
    Change in axial length as measured by non-contact axial length both eyes, will be measured at baseline and at one year to assess the difference in change in axial length between the treatment group (multifocal toric soft contact lens) and the control group (toric soft contact lens)

    Secondary Outcome Measures

    Full Information

    First Posted
    April 15, 2020
    Last Updated
    November 5, 2020
    Sponsor
    University of Alabama at Birmingham
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04352868
    Brief Title
    Customizing Myopia Control With Multifocal Toric Contact Lens
    Official Title
    Customizing Myopia Control With Multifocal Toric Contact Lens
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2020
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    COVID-19
    Study Start Date
    September 1, 2020 (Anticipated)
    Primary Completion Date
    September 1, 2021 (Anticipated)
    Study Completion Date
    September 1, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Alabama at Birmingham

    4. Oversight

    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
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This study will evaluate the ability of toric multifocal contact lens to reduce the change of myopia progression in children (aged 8-12) with myopic astigmatism.
    Detailed Description
    The purpose of this study is to assess if a center distance toric multifocal contact lenses can slow the amount of change of myopia progression in children with myopia plus astigmatism. Multifocal contact lenses have been theorized to influence the peripheral optics of the eye such that they slow the rate of myopia progression in nearsighted children. This outcome is yet to be evaluated in children with myopia plus astigmatism.The secondary outcome is to measure the change in peripheral optics caused by the contact lens. This information is key to understanding the mechanism of multifocal contact lens optics on the eye. Ultimately this information would be used to create a software that can estimate the effect of multifocal contact lenses on the peripheral optics of the child's eye. This software can potentially be used by practitioners worldwide to better customize multifocal contact lenses to slow myopia progression.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Refractive Errors, Myopia
    Keywords
    Myopia, Multifocal contact lens, Refractive error, Myopia treatment, Myopia control, Myopia management

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Toric soft contact lens
    Arm Type
    Active Comparator
    Arm Description
    Toric soft contact lens
    Arm Title
    Multifocal toric soft contact lens
    Arm Type
    Experimental
    Arm Description
    A multifocal toric soft contact lens with a +2.00 D add.
    Intervention Type
    Device
    Intervention Name(s)
    Intelliwave multifocal, toric, soft contact lens
    Intervention Description
    This is a quarterly disposable, multifocal, toric soft contact lens commercially available from Art Optical Contact Lens, Inc.
    Intervention Type
    Device
    Intervention Name(s)
    Intelliwave toric, soft contact lens
    Intervention Description
    This is a quarterly disposable toric soft contact lens commercially available from Art Optical Contact Lens, Inc.
    Primary Outcome Measure Information:
    Title
    Refractive error progression
    Description
    Refractive error measured by cycloplegic autorefraction in both eyes, will be measured at baseline and at one year to assess the difference in spherical component of the refractive error between the treatment group (multifocal toric soft contact lens) and the control group (toric soft contact lens)
    Time Frame
    1 years
    Title
    Axial length
    Description
    Change in axial length as measured by non-contact axial length both eyes, will be measured at baseline and at one year to assess the difference in change in axial length between the treatment group (multifocal toric soft contact lens) and the control group (toric soft contact lens)
    Time Frame
    1 years

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    8 Years
    Maximum Age & Unit of Time
    12 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: 8 to 12 years, inclusive, at baseline examination -0.50 to -6.00 D, inclusive, spherical component, cycloplegic autorefraction ≥0.75 DC, cycloplegic autorefraction 0.1 logMAR or better best-corrected visual acuity in each eye Exclusion Criteria: Eye disease or refractive error conditions (e.g., keratoconus, retinal abnormalities, retinopathy of prematurity, etc.) Ocular surgery, severe ocular trauma, active ocular infection or inflammation Subjects with a condition or in a situation, which in the examiner's opinion, may put the subject at significant risk, may confound the study results, or may significantly interfere with their participation in the study.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Andrew D Pucker, OD, PhD
    Organizational Affiliation
    University of Alabama at Birmingham
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    There is no plan to share individual subject data.

    Learn more about this trial

    Customizing Myopia Control With Multifocal Toric Contact Lens

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