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A Prospective Safety and Effectiveness Study of a New High Repetition Rate Excimer Laser Using LASIK for the Correction of Ammetropia and Presbyopia

Myopia Clinical Trial

Clinical Trial Summary

This clinical study has been planned to evaluate the safety and effectiveness of common treatment algorithms using 500 Hz laser repetition rate for the correction of Ammetropia and Presbyopia

Clinical Trial Description

This clinical study has been planned to evaluate the safety and effectiveness of the excimer laser treatment algorithms Proscan, Zyoptix and Supracor of the 500 Hz laser system for ametropia and/or presbyopia when performed on the cornea of virgin eyes. ;

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02112968
Study type Interventional
Source Technolas Perfect Vision GmbH
Contact Melanie Doerner
Phone +49 89 94004130
Email melanie.doerner@bausch.com
Status Not yet recruiting
Phase Phase 4
Start date December 2014
Completion date May 2017
View Details
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