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Myopia:the Role of Cone Opsin Mutations & Glasses That Control Axial Elongation

Primary Purpose

Myopia

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Spectacles with red-blocking tint
Spectacles with holographic diffuser and color neutral tint
Spectacles with holographic diffuser and red-blocking tint
Spectacles with color neutral tint
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Myopia focused on measuring myopia, nearsightedness, axial elongation of the eye, refractive error

Eligibility Criteria

8 Years - 13 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • nearsighted having a refractive error of at least -0.5 diopters
  • myopia progression at least -.50 D per year in previous year
  • astigmatism and anisometropia not more than 1.5 D
  • distance monocular acuity 6/6 or better
  • near monocular acuity of 0.4 M or better
  • stereoacuity not more than 40 sec of arc at 40 cm
  • able to respond to subjective testing
  • no contact lens use during the study
  • able to comply with wearing the experimental lenses daily for 18 months
  • able to have axial length measurements accurately on the Zeiss Intraocular Lens Master
  • willing to donate a blood sample or a buccal swab for genetic analysis
  • can be refracted to 20/20 or 20/15

Exclusion Criteria:

  • glaucoma, amblyopia, strabismus
  • ocular disease
  • developmental delay
  • history of wearing bifocal lenses
  • any type of eye surgery
  • color vision deficiency

Sites / Locations

  • University of Washington

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Other

Other

Other

Arm Label

color blocking tint

holographic diffuser

diffuser & color blocking tint

holographic diffuser and neutral tint

Arm Description

Spectacles with red-blocking tint subjects will wear glasses daily for 6 months and have

Spectacles with color neutral tint subjects will wear glasses daily for 6 months and have

Spectacles with holographic diffuser and red-blocking tint subjects will wear glasses daily for 6 months and have

Spectacles with holographic diffuser and color neutral tint subjects will wear glasses daily for 6 months and have

Outcomes

Primary Outcome Measures

Myopia progression measured by rate of axial elongation of the eye
The axial length of both eyes will be measured before wearing the experimental eyeglasses, then once every three months thereafter for 18 months, and again 6 months after subjects stop wearing the study eye glasses. The rate of axial elongation will be calculated.

Secondary Outcome Measures

Myopia progression measured by cycloplegic autorefraction.
A cycloplegic autorefraction will be done at the beginning of the study before subjects start wearing the study glasses, after 18 months of wearing the study glasses,and again about 6 months after wearing the study glasses stopped.

Full Information

First Posted
August 13, 2013
Last Updated
August 12, 2019
Sponsor
University of Washington
Collaborators
Seattle Children's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01923675
Brief Title
Myopia:the Role of Cone Opsin Mutations & Glasses That Control Axial Elongation
Official Title
Myopia:the Role of Cone Opsin Mutations & Glasses That Control Axial Elongation
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Withdrawn
Why Stopped
no funding
Study Start Date
November 2013 (Anticipated)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Seattle Children's Hospital

4. Oversight

5. Study Description

Brief Summary
To determine the effect of spectacles with a red blocking filter on myopia progression in children. To determine the effect of spectacles with a holographic diffuser that spreads incident light rays over an angle of 0.5 degrees on myopia progression in children To determine the combined effects of spectacles with a red blocking filter and a diffuser that spreads incident light over an angle of 0.5 degrees on myopia progression in children.
Detailed Description
In this clinical trial we will determine whether commercially available lens tints that are normally used for cosmetic purposes or for blocking sunlight have a beneficial effect of slowing axial eye growth in children with myopia when used alone or in conjunction with a holographic diffuser that blurs the image slightly. The following procedures will be performed on a total of 240 children from 8 to 13 years of age: Color vision tests (Richmond Hardy-Rand-Rittler pseudoisochromatic plate test and/or the Rayleigh match test and/or the Neitz Test of Color Vision), and machine-based vision tests using the Titmus tester (color vision, binocularity, acuity, and heterophoria tests); each subject will provide a blood sample or a buccal swab for genetic analysis of the long and middle wavelength cone photopigment genes in order to determine the relationship between the cone opsins and myopia; eye measurements including axial length and corneal curvature will be performed using the Zeiss Intraocular Lens Master; cycloplegic autorefraction will be doe at the beginning of the study before participants start wearing the study spectacles, after 18 months if wearing the study spectacles, and 6 months after participants stop wearing the study spectacles. 4) subjects will be randomly assigned to one of four groups, consisting of 60 subjects each, each group will be assigned one of four study spectacles. The study spectacles for all participants will have the optimal lens corrections for both eyes. Group 1 participants will wear spectacles with lenses tinted to blocks red light. Group 2 participants will wear spectacles with lenses that have a holographic diffuser on surface of and that are tinted to reduce the light intensity by the same amount that the red-blocking tint does. Group 3 participants will wear spectacles that are tinted to block red light and that have a holographic diffuser. Group 4 participants will wear spectacles that are tinted to reduces the light intensity by the same amount that the red-blocking tint does. Participants will wear the study glasses for 18 months. Axial length measurements will be taken twice prior to when subjects begin wearing the glasses and once every three month thereafter.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myopia
Keywords
myopia, nearsightedness, axial elongation of the eye, refractive error

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
color blocking tint
Arm Type
Experimental
Arm Description
Spectacles with red-blocking tint subjects will wear glasses daily for 6 months and have
Arm Title
holographic diffuser
Arm Type
Other
Arm Description
Spectacles with color neutral tint subjects will wear glasses daily for 6 months and have
Arm Title
diffuser & color blocking tint
Arm Type
Other
Arm Description
Spectacles with holographic diffuser and red-blocking tint subjects will wear glasses daily for 6 months and have
Arm Title
holographic diffuser and neutral tint
Arm Type
Other
Arm Description
Spectacles with holographic diffuser and color neutral tint subjects will wear glasses daily for 6 months and have
Intervention Type
Other
Intervention Name(s)
Spectacles with red-blocking tint
Intervention Description
Eyeglasses will have lenses that will correct refractive error for each subject, and will have a tint that blocks red light.
Intervention Type
Other
Intervention Name(s)
Spectacles with holographic diffuser and color neutral tint
Intervention Description
Eyeglasses will correct refractive error for each subject but will have a holographic diffuser applied to the surface and will have a color neutral filter to adjust the light intensity reaching the eyes to be the same as for groups 1 and3.
Intervention Type
Other
Intervention Name(s)
Spectacles with holographic diffuser and red-blocking tint
Intervention Description
Eyeglasses will correct refractive error for each subject and will be tinted to block red light, and will have a holographic diffuser to blur the image.
Intervention Type
Other
Intervention Name(s)
Spectacles with color neutral tint
Intervention Description
Eyeglasses will correct refractive error for each subject and will have a color neutral tint to adjust the light intensity reaching the eyes so it is the same as for groups 1 and 3.
Primary Outcome Measure Information:
Title
Myopia progression measured by rate of axial elongation of the eye
Description
The axial length of both eyes will be measured before wearing the experimental eyeglasses, then once every three months thereafter for 18 months, and again 6 months after subjects stop wearing the study eye glasses. The rate of axial elongation will be calculated.
Time Frame
every 3 months for 18 months
Secondary Outcome Measure Information:
Title
Myopia progression measured by cycloplegic autorefraction.
Description
A cycloplegic autorefraction will be done at the beginning of the study before subjects start wearing the study glasses, after 18 months of wearing the study glasses,and again about 6 months after wearing the study glasses stopped.
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: nearsighted having a refractive error of at least -0.5 diopters myopia progression at least -.50 D per year in previous year astigmatism and anisometropia not more than 1.5 D distance monocular acuity 6/6 or better near monocular acuity of 0.4 M or better stereoacuity not more than 40 sec of arc at 40 cm able to respond to subjective testing no contact lens use during the study able to comply with wearing the experimental lenses daily for 18 months able to have axial length measurements accurately on the Zeiss Intraocular Lens Master willing to donate a blood sample or a buccal swab for genetic analysis can be refracted to 20/20 or 20/15 Exclusion Criteria: glaucoma, amblyopia, strabismus ocular disease developmental delay history of wearing bifocal lenses any type of eye surgery color vision deficiency
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jay Neitz, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98109
Country
United States

12. IPD Sharing Statement

Citations:
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15545808
Citation
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PubMed Identifier
14558848
Citation
Grosvenor T. Why is there an epidemic of myopia? Clin Exp Optom. 2003 Sep;86(5):273-5. doi: 10.1111/j.1444-0938.2003.tb03122.x. No abstract available.
Results Reference
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PubMed Identifier
12657584
Citation
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Myopia:the Role of Cone Opsin Mutations & Glasses That Control Axial Elongation

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