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Clinical Trial Summary

The objectives of this study are to evaluate the safety and efficacy, with regards to regression of refractive outcome, as measured by manifest refraction spherical equivalent (MRSE), of two treatment regimens for hyperopic and hyperopic astigmatic subjects: LASIK followed by cross-linking performed with the KXL System and Photrexa ZD™ (Riboflavin Ophthalmic Solution), as compared to LASIK alone.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01893359
Study type Interventional
Source Glaukos Corporation
Contact
Status Terminated
Phase Phase 1/Phase 2
Start date August 2013
Completion date April 2016

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