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Clinical Trials/NCT03358862
NCT03358862
Unknown
Not Applicable

Myopia Progression in Children and Adolescents Before and After Use of a Novel Extended Depth of Focus Daily Disposable Soft Contact Lens

Aller, Thomas A., OD1 site in 1 country80 target enrollmentJanuary 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myopia
Sponsor
Aller, Thomas A., OD
Enrollment
80
Locations
1
Primary Endpoint
Refractive error changes
Last Updated
5 years ago

Overview

Brief Summary

Myopia has been increasing in prevalence and severity throughout the world over the last 30 years. Increasing levels of myopia are associated with increased frequencies and severity of various ocular pathologies, including cataracts, glaucoma, retinal detachments and other retinal pathologies and myopic maculopathy. Slowing myopia progression at a young age before the eye reaches excessive axial length may help to reduce the future risks of these ocular pathologies.

Conventional spectacles and contact lenses are prescribed correct myopia by moving the central focus of the eye for distance viewing from in front of the retina to on the retina centrally, or at the fovea. To varying degrees, these lenses allow the light to focus behind the retina, at varying peripheral retinal locations. These findings have led to efforts to design spectacle and contact lenses which correct peripheral hyperopic defocus, to reduce myopia progression.

The consensus theory for how both multifocal contact lenses and orthokeratology can control myopia progression is that they each can reduce, eliminate, or reverse relative peripheral hyperopic defocus. Existing published studies on the use of multifocal contact lenses to control myopia in humans have utilized lenses with the distance correction in the center with peripheral plus power to correct the peripheral blur. Until recently, there have been no daily disposable multifocal lenses in the US market with distance center designs.

The NaturalVue contact lens from Visioneering Technologies, Inc. is the first daily disposable distance center multifocal in the US. It has a novel extended depth of focus design where the distance correction is in the center of the optical zone, surrounded by a zone characterized by having a seamless, rapid transition from the distance power to a highly plus power at the edge of the optical zone.

This study will analyze the myopia progression of patients in the investigator's practice while wearing their habitual visual corrections for periods up to two years prior to being switched to NaturalVue contact lenses. They will then be followed for up to two years after beginning use of this novel lens design and the differences in their myopia progression after versus before this novel lens will be analyzed. Axial lengths will be measured with the IOLMaster after switching to NaturalVue, at six-month intervals and will be compared to axial lengths which have been collected with habitual corrections.

Detailed Description

Myopia has been increasing in prevalence and severity throughout the world over the last 30 years. Increasing levels of myopia are associated with increased frequencies and severity of various ocular pathologies, including cataracts, glaucoma, retinal detachments and other retinal pathologies and myopic maculopathy. Slowing myopia progression at a young age before the eye reaches excessive axial length may help to reduce the future risks of these ocular pathologies. Conventional spectacles and contact lenses are prescribed to correct myopia by moving the central focus of the eye for distance viewing from in front of the retina to on the retina centrally, or at the fovea. To varying degrees, these lenses allow the light to focus behind the retina, at varying peripheral retinal locations. These findings have led to efforts to design spectacle and contact lenses which correct peripheral blur to reduce myopia progression. The consensus theory for how both multifocal contact lenses and orthokeratology can control myopia progression is that they each can reduce, eliminate, or reverse relative peripheral hyperopic defocus. Existing published studies on the use of multifocal contact lenses to control myopia in humans have utilized lenses with the distance correction in the center with peripheral plus power to correct the peripheral hyperopic defocus. Until recently, there have been no daily disposable multifocal lenses in the US market with distance center designs. The NaturalVue contact lens from Visioneering Technologies, Inc. is the first daily disposable distance center multifocal in the US. It has a novel extended depth of focus design where the distance correction is in the center of the optical zone, surrounded by a zone with a seamless, rapid transition from the distance power to a highly plus power at the edge of the optical zone. This study will analyze the myopia progression of patients in the investigator's practice while wearing their habitual visual corrections for periods up to two years prior to being switched to NaturalVue contact lenses. They will then be followed for up to two years after beginning use of this novel lens design and the differences in their myopia progression after NaturalVue versus before NaturalVue will be analyzed. Axial lengths will be measured with the IOLMaster after switching to NaturalVue, at six-month intervals and will be compared to axial lengths which have been collected with habitual corrections.

Registry
clinicaltrials.gov
Start Date
January 1, 2017
End Date
July 1, 2022
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Aller, Thomas A., OD
Responsible Party
Principal Investigator
Principal Investigator

Thomas A. Aller, OD

Principal Investigator

Aller, Thomas A., OD

Eligibility Criteria

Inclusion Criteria

  • Myopic refractive error
  • Astigmatism less than -2.50 D
  • Evidence from clinical record of myopia progression equal to or greater than -0.50 D in at least one eye since the prior examination
  • Ability to see 20/30 or better in the worse eye and 20/25 or better binocularly after one week adaptation
  • Ability to properly insert, remove and care for study lens

Exclusion Criteria

  • Moderate to severe allergic conjunctivitis
  • Moderate to severe dry eyes
  • Keratoconus or other related corneal irregularity
  • Strabismus
  • Amblyopia
  • Nystagmus

Outcomes

Primary Outcomes

Refractive error changes

Time Frame: Data will be collected at baseline and at every six months.

Changes in myopia over time will be characterized by the spherical equivalent refractive error as measured by manifest subjective refraction.

Axial length of the eye

Time Frame: Data will be collected at baseline and at every six months.

Changes in the axial length of the eye will be measured with the Zeiss IOLMaster

Secondary Outcomes

  • Corneal curvature(Data will be collected at baseline and at every six months)
  • Vitreous Chamber Depth(Data will be collected at baseline and at every six months.)

Study Sites (1)

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