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
| Type | Name | Description |
|---|---|---|
| DRUG | Atropine | Compare 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.