ODSEEH: Optical Defocus to Stimulate Eye Elongation in Hyperopia

Sponsor
Aller, Thomas A., OD (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT00950924
Collaborator
(none)
30
1
2
84
0.4

Study Details

Study Description

Brief Summary

Axial hyperopia results when the length of the eye is too short for the eye to properly focus distance objects on the retina while the focusing system is relaxed. Emmetropization is the process by which the eye actively adjusts various components of the eye to gradually improve the focus of the eye. Emmetropization frequently involves either an increase or a decrease in the growth of the eye, particularly during infancy and childhood. Numerous animal studies suggest that if an animal is exposed to retinal images located behind the retina either centrally or peripherally, the eye will grow in the direction of the focused image. If an abnormally short eye has resulted in hyperopia, exposing such an eye to retinal images partially located behind the retina might encourage axial elongation, thus reducing the hyperopia.

Condition or Disease Intervention/Treatment Phase
  • Device: Simultaneous Vision Bifocal Soft Contact Lenses
  • Device: Single Vision Soft Contact Lenses
N/A

Detailed Description

Hyperopia or farsightedness may cause distance vision and near vision to be blurred. Depending on the severity of the condition and the age of the patient and the status of the binocular vision system, hyperopia can also cause fatigue, asthenopia, headaches, double vision, and amblyopia. Low to moderate amounts of hyperopia rarely cause much difficulty in the young person, but will eventually cause significant near vision problems as the patient ages. Hyperopia can be caused by the eye being too short (axial hyperopia) or by the cornea being too flat or the crystalline lens being to weak (refractive hyperopia). It has been established by the PI that axial growth can be dramatically lessened in children and adolescents with myopia through the use of bifocal contact lenses prescribed in a particular way (The CONTROL Study). Studies by Earl Smith, O.D., Ph.D. have suggested that multi-zonal contact lenses that provide proper axial focus while manipulating peripheral defocus can either discourage or encourage axial growth to treat myopia or hyperopia respectively. In the present study, simultaneous vision bifocal soft contact lenses will be used to encourage axial growth in hyperopic children and adolescents with axial hyperopia in an effort to reduce hyperopia. Subjects will be randomly assigned to wear either bifocal soft contact lenses or single vision soft lenses. The bifocal contact lenses will be prescribed to provide for clear central vision at both distance and near with the near zone of the contact, thus exposing the retina to hyperopic defocus from the distance zone.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Treatment
Official Title:
Use of Multifocal Contact Lenses to Stimulate Axial Elongation in Axial Hyperopia
Study Start Date :
Jan 1, 2015
Anticipated Primary Completion Date :
Oct 1, 2021
Anticipated Study Completion Date :
Jan 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Bifocal Contact Lenses

Simultaneous Vision Bifocal Soft Contact Lenses will be prescribed such that the distance vision as measured by manifest subjective refraction will be properly corrected by the near vision add power and undercorrected by the distance power.

Device: Simultaneous Vision Bifocal Soft Contact Lenses
Simultaneous Vision Bifocal Soft Contact Lenses will be prescribed such that the distance vision as measured by manifest subjective refraction will be properly corrected by the near vision add power and undercorrected by the distance power.

Placebo Comparator: Single Vision Soft Contact Lenses

Subjects will be fitted with single vision soft contact lenses with goal of corrected emmetropia at a distance of 20 feet.

Device: Single Vision Soft Contact Lenses
Single vision soft contact lenses will be prescribed to properly correct the distance vision as measured by manifest subjective refraction.

Outcome Measures

Primary Outcome Measures

  1. Axial length [One year]

Secondary Outcome Measures

  1. Refractive Error [One year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
5 Years to 12 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Aged 5-12

  • Hyperopia > +1.25 each eye (cycloplegic refraction)

  • Ability to wear soft contact lenses

Exclusion Criteria:
  • Amblyopia

  • Strabismus

  • Astigmatism > 1.00 diopters

  • Axial Length > 24.00 mm

Contacts and Locations

Locations

Site City State Country Postal Code
1 711 Kains Ave San Bruno California United States 94066

Sponsors and Collaborators

  • Aller, Thomas A., OD

Investigators

  • Principal Investigator: Thomas A Aller, O.D., Unafilliated

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Aller, Thomas A., OD
ClinicalTrials.gov Identifier:
NCT00950924
Other Study ID Numbers:
  • NCT00950924
First Posted:
Aug 3, 2009
Last Update Posted:
Jan 12, 2021
Last Verified:
Jan 1, 2021
Keywords provided by Aller, Thomas A., OD
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 12, 2021