Clinical Trials Directory

Trials / Completed

CompletedNCT02130167

Low Concentration Atropine for Myopia Progression in School Children

Low Concentrations of Atropine for Controlling Myopia Progression in School Children

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Chang Gung Memorial Hospital · Academic / Other
Sex
All
Age
6 Years – 12 Years
Healthy volunteers
Not accepted

Summary

Myopia is the leading cause of blindness in Taiwan. The younger children with myopia, the higher risk of high myopia in later life and complications such as retinal detachment and maculopathy will occur. We have reported the low concentration of atropine (0.05%) with the effect on retarding the myopia progression. Recently the 0.01% atropine was also reported effective and with less visual side effects such as mydriasis. The aim of this study is to compare the efficacy in controlling myopia progression and visual side effects of 2 low concentration of atropine(0.05% vs 0.01%) in children aged 6-12 years with myopia of at least -0.5 diopters (D) and astigmatism of -1.50 D or less.

Conditions

Interventions

TypeNameDescription
DRUGAtropineCompare different concentrations of atropine eye drops (0.01% vs 0.05%) in the efficacy of controlling myopia progression and side effects of atropine

Timeline

Start date
2012-08-01
Primary completion
2017-07-01
Completion
2017-08-01
First posted
2014-05-05
Last updated
2018-01-30

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT02130167. Inclusion in this directory is not an endorsement.