Optical Defocus to Stimulate Eye Elongation in Hyperopia (ODSEEHyperopia)
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Purpose
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 | Intervention |
|---|---|
|
Hyperopia Refractive Error |
Device: Simultaneous Vision Bifocal Soft Contact Lenses Device: Single Vision Soft Contact Lenses |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator) Primary Purpose: Treatment |
| Official Title: | Use of Multifocal Contact Lenses to Stimulate Axial Elongation in Axial Hyperopia |
- Axial length [ Time Frame: One year ] [ Designated as safety issue: No ]
- Refractive Error [ Time Frame: One year ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 30 |
| Study Start Date: | December 2011 |
| Estimated Study Completion Date: | March 2013 |
| Estimated Primary Completion Date: | June 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Bifocal Contact Lenses
Subjects will be fitted with bifocal contact lenses with a simultaneous vision type design.
|
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 6M.
|
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.
|
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, OD, PhD 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.
Eligibility| Ages Eligible for Study: | 7 Years to 25 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Aged 7-25
- 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| Contact: Thomas A Aller, O.D. | 6508711816 | cptreyes@earthlink.net |
| United States, California | |
| 711 Kains Ave | Not yet recruiting |
| San Bruno, California, United States, 94066 | |
| Contact: Thomas A Aller, O.D. 650-871-1816 cptreyes@earthlink.net | |
| Principal Investigator: Thomas A Aller, O.D. | |
| Principal Investigator: | Thomas A Aller, O.D. | Unafilliated |
More Information
No publications provided
| Responsible Party: | Thomas Aller, OD, Dr. Thomas Aller Optometrist, Inc. |
| ClinicalTrials.gov Identifier: | NCT00950924 History of Changes |
| Other Study ID Numbers: | NCT07312009 |
| Study First Received: | July 30, 2009 |
| Last Updated: | July 25, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Aller, Thomas A., OD:
|
Hyperopia Refractive Error Ocular Biometrics |
Axial Length Contact Lenses Bifocal Contact Lenses |
Additional relevant MeSH terms:
|
Hyperopia Refractive Errors Eye Diseases |
ClinicalTrials.gov processed this record on May 21, 2013