Objective: to evaluate the efficacy of different concentrations of atropine eye drops in controlling the progression (diopter, axial length) of high myopia in young children, and to compare the compliance, adverse reaction and regression rate of different concentrations of atropine eye drops in myopia control. Intervention: Group 1 (0.01% atropine group), Group 2 (0.04% atropine group), Group 3 (0.1% atropine group). During the 2-year intervention period after entering the group, each concentration of atropine eye drops were given every night at a fixed time before going to bed, one drop each time, implemented by parents (supervision), and the wechat small program was completed.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Enrollment
357
different concentrations (0.01%/0.04%/0.1%) of atropine were administered to high myopic children
Shanghai Eye Disease Prevention & Treatment Center
Shanghai, Shanghai Municipality, China
RECRUITINGShanghai General Hospital
Shanghai, China
RECRUITINGShanghai Ninth People's Hospital
Shanghai, China
RECRUITINGchanges of spherical equivalent
Spherical equivalent as measured by cycloplegia autorefraction
Time frame: at least 3 years
changes of axial length
AL was measured as the distance from the anterior corneal surface to the retinal pigment epithelium (RPE) using IOLMaster or Lenstar
Time frame: at least 3 years
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