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Clinical Trial Summary

This study will evaluate the efficacy and safety of posterior scleral reinforcement on controlling myopia progression, including change in refraction, axial elongation as well as sight-threatening complications, in adults with high myopia. Half the adults will receive posterior scleral reinforcement, while the other half will receive no surgerical treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03381079
Study type Interventional
Source Beijing Tongren Hospital
Contact Shi-Ming Li, PhD
Phone +86-10-58269920
Email lishiming81@163.com
Status Not yet recruiting
Phase Phase 2
Start date April 1, 2018
Completion date December 31, 2020

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