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Clinical Trial Summary

To evaluate the effect of early vision screening with automated photorefraction device in high risk children


Clinical Trial Description

Pre-term, low-birth-weight, and development delay are well-known risk factors related to higher incidence of high refractive error and strabismus, which can potentially lead to amblyopia and is regarded as amblyopia risk factors. This project is a cross-sectional controlled study. Our study includes high-risk group and normal group. High-risk group includes children with birth history of pre-term, low-birth-weight and the diagnosis of development delay in FEMH. Normal group enrolled age-matched children without those risk factors. Vision screening by FDA-approved photorefraction device as well as comprehensive ophthalmic exams for definite diagnosis will be performed on the high-risk group and the normal group. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02678468
Study type Observational
Source Far Eastern Memorial Hospital
Contact Yao-Lin Liu, M.D.
Phone 886-289667000
Email liuyaolin.tw@gmail.com
Status Recruiting
Phase N/A
Start date February 2016
Completion date March 2018

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