Clinical Trials Directory

Trials / Completed

CompletedNCT00787579

Assessment of Bifocal and Prismatic Bifocal Spectacles for Myopia Control in Children

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
135 (actual)
Sponsor
Essilor International · Industry
Sex
All
Age
8 Years – 13 Years
Healthy volunteers
Accepted

Summary

1. To determine if the effect of near-addition lenses (bifocals) is more prominent for children with high myopia progression. 2. To study how different subject characteristics such as age, gender, baseline degree of myopia, baseline near phoria and baseline lag of accommodation affect the efficacy of bifocal lens wear in myopic children. 3. To investigate the effect of incorporating near base-in prisms along with the near-addition lenses (prismatic bifocals) on myopia progression in myopic children.

Conditions

Interventions

TypeNameDescription
DEVICEBifocal spectacles+1.50D bifocal spectacles
DEVICEPrismatic bifocal spectacles+1.50D bifocal spectacles combined with 3Δ base-in prisms

Timeline

Start date
2003-04-01
Primary completion
2008-04-01
First posted
2008-11-07
Last updated
2008-11-07

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00787579. Inclusion in this directory is not an endorsement.

Assessment of Bifocal and Prismatic Bifocal Spectacles for Myopia Control in Children (NCT00787579) · Clinical Trials Directory