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A Study Raindrop Near Vision Inlay in Presbyopes Implanted in Corneal Pockets

Presbyopia Clinical Trial

Official title:
A Prospective Study to Evaluate the Raindrop Near Vision Inlay in Presbyopes Implanted in Corneal Pockets With a Delayed or Non-Delayed Approach

Clinical Trial Summary

The objective of this study is to evaluate the Raindrop® Near Vision Inlay for the improvement of near vision in presbyopes implanted in corneal pockets with a delayed or a non-delayed approach.

Clinical Trial Description

Patients must be presbyopic with a reading add from +1.5 to +2.5 D, and both emmetropes (MRSE from -0.5 to +0.5 D) as well as ametropes (requiring concurrent LASIK) are included in the investigation. In the non-delayed approach, the corneal pocket is created and inlay implanted on the same surgical day. In the delayed approach, the corneal pocket is created and dissected but the corneal inlay is not implanted. After one to three months, the corneal inlay is implanted on a second surgical day. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03326869
Study type Interventional
Source Eye Center of North Florida
Contact
Status Terminated
Phase N/A
Start date October 18, 2017
Completion date October 23, 2018
View Details
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