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Exploratory Clinical Study for Techniques Associated With the Fluid Accommodating IOL

Presbyopia Clinical Trial

Official title:
Exploratory Clinical Study for Techniques Associated With the Fluid Accommodating IOL

Clinical Trial Summary

The purpose of this clinical study is to assess the repeatability of objective refraction using auto refraction on subjects bilaterally implanted (implanted in both eyes) with the Fluid Accommodating IOL (FAIOL).

Clinical Trial Description

Subjects will be expected to attend 10 office visits from screening to exit. The total expected duration of participation for each subject in this study is approximately 12 months. The second eye surgery will take place within 7-15 days from the date of the first implanted eye. The primary endpoint will be collected at Month 1, following the 2nd eye implant date. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04330001
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date December 28, 2020
Completion date May 3, 2023
View Details
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