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Clinical Trial Summary

The primary objective of this study is to conduct a post-approval study which compares the LAL to a monofocal control IOL for safety outcomes.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05202808
Study type Interventional
Source RxSight, Inc.
Contact David B Goffredo
Phone 9494215463
Email [email protected]
Status Recruiting
Phase N/A
Start date December 3, 2021
Completion date December 2024

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