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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00214487
Other study ID # CR-0107
Secondary ID
Status Completed
Phase N/A
First received September 14, 2005
Last updated June 23, 2014
Start date October 2003
Est. completion date March 2006

Study information

Verified date June 2014
Source Aller, Thomas A., OD
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether bifocal soft contact lenses are effective in controlling the progression of myopia in children and adolescents that exhibit a tendency to excessively cross their eyes while reading (esophoria or eso fixation disparity). Several studies have demonstrated that bifocal or progressive multifocal spectacles are effective in slowing the progression of myopia in children either with near point esophoria and/or with inadequate focusing at near. A prominent theory for one cause of myopia progression is that poorly focused images on the back of the eye (retina) cause the eye to lengthen, causing an increase in myopia. Bifocal contact lenses may reduce this retinal defocus, reducing the stimulus to eye elongation, and thus may reduce myopia progression.


Description:

Myopia has become the focus of growing attention and concern because the prevalence of myopia appears to increasing in some populations (reaching 90% for some university student populations in Asia). There are serious risks to higher levels of myopia, including cataracts, glaucoma, retinal detachment and myopic retinal degeneration. Several studies have shown mild to moderate control of myopia progressionwith bifocal or multifocal spectacles in children with esophoria at near and/or with accommodative deficiencies. Pilot studies by the P.I. have suggested that bifocal contact lenses may control myopia progression in children with near point eso fixation disparity.

CONTROL is a controlled, randomized, prospective, double-blind, one year study of the changes in myopia in 80-90 subjects from age 8-18 with low to moderate levels of myopia, low levels of astigmatism, and eso fixation disparity at near, when fitted with either bifocal soft contact lenses or single vision soft contact lenses. The primary outcome measures will be cycloplegic refraction and axial length measures.


Recruitment information / eligibility

Status Completed
Enrollment 78
Est. completion date March 2006
Est. primary completion date March 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 8 Years to 18 Years
Eligibility Inclusion Criteria:

- Myopia between -0.50 and -6.00

- Eso fixation disparity at 33cm with distance correction

- Astigmatism 1.00 or less

- Ability to wear soft contact lenses

Exclusion Criteria:

- Presence of ocular disease preventing wear of contacts

- Pregnancy or nursing

- Use of certain medications

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Device:
Bifocal Contact Lenses
Use of bifocal contact lenses of varying add powers to control the progression of myopia
Placebo Control
Single vision soft contact lenses

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Aller, Thomas A., OD Johnson & Johnson Vision Care, Inc.

References & Publications (4)

Aller TA, Wildsoet C. Bifocal soft contact lenses as a possible myopia control treatment: a case report involving identical twins. Clin Exp Optom. 2008 Jul;91(4):394-9. doi: 10.1111/j.1444-0938.2007.00230.x. Erratum in: Clin Exp Optom. 2008 Sep;91(5):479. — View Citation

Aller TA, Wildsoet C. Results of a one-year prospective clinical trial (CONTROL) of the use of bifocal soft contact lenses to control myopia progression. Ophthalmic and Physiological Optics 26(S1), 8-9.

Aller TA. Design of a prospective clinical trial of the use of bifocal soft contact lenses to control myopia progression (CONTROL). Proceedings of the 10th International Myopia Conference 2004:29.

Tarrant J, Severson H, Wildsoet CF. Accommodation in emmetropic and myopic young adults wearing bifocal soft contact lenses. Ophthalmic Physiol Opt. 2008 Jan;28(1):62-72. doi: 10.1111/j.1475-1313.2007.00529.x. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in Cycloplegic Autorefraction in One Year. One year No
Secondary Keratometric Changes at One Year. One year No
Secondary Changes in Manifest Refraction at One Year. One year No
Secondary Relationship Between Residual Fixation Disparity and Myopia Progression. One year No
Secondary Changes in Cycloplegic Subjective Refraction in One Year One year No
Secondary Changes in Axial Length at One Year. One year No
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