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Wavefront-guided LASIK for Monovision Treatment of Myopic Subjects With Presbyopia

Refractive Error Clinical Trial

Official title:
Post-approval Study of Wavefront-guided LASIK for Monovision Treatment of Myopic Subjects With Presbyopia

Clinical Trial Summary

This study will be a 12-month, prospective, multicenter, open-label, non-comparative, non-randomized clinical investigation conducted at 8 to 14 sites. A total of 383 subjects will be enrolled to achieve approximately 268 treated subjects, resulting in at least 241 evaluable subjects at the point of refractive stability. After signing the informed consent, subjects meeting all inclusion and exclusion criteria in both eyes may be scheduled for surgery. The follow-up visit schedule will be the same for each operative eye.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04075591
Study type Interventional
Source AMO Development, LLC
Contact Study Contact
Phone +1 949 7042580
Email DParizad@ITS.JNJ.com
Status Recruiting
Phase N/A
Start date September 24, 2019
Completion date April 30, 2026
View Details
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