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Effects of Low Concentration Atropine on Pupillary Size and Accommodative Amplitude

Myopia Clinical Trial

Official title:
Evaluation of Two-week Effects of 0.01%, 0.02% and 0.03% Atropine Eye Drops on Children Eyes With Myopia

Clinical Trial Summary

To assess the two-week ocular responses, especially on pupillary size and accommodative amplitude, of nightly application of 0.01% or 0.02% or 0.03% atropine eye drops in children with myopia who were randomized to use of three different low-concentration atropine eye drops

Clinical Trial Description

Atropine was proven to be effective in controlling myopia progression. However, the most common side effects of the use of atropine eye drop are dilation of pupil and decrease of accommodation. The investigators wish to evaluate the ocular responses of three low concentration atropine eye drops, 0.01% or 0.02% or 0.03%, mainly on the pupillary size and accommodative responses in children aged between 6 to 12 years old over two-week usage. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03699423
Study type Interventional
Source Hai Yen Eye Care
Contact
Status Completed
Phase Phase 1
Start date March 8, 2018
Completion date April 30, 2018
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