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Withdrawn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
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
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
NCT ID
NCT04352868
First Posted
April 15, 2020
Last Updated
November 5, 2020
Sponsor
University of Alabama at Birmingham
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
We'll reach out to this number within 24 hrs