Feasibility Study of an Accommodating IOL Design

Recruiting N/A Interventional Study
Aphakia
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
22 and older
Sex
Any
Study type
Interventional
Purpose
Device Feasibility
Participants needed
85 (estimated)
Sponsor
Alcon Research · Industry
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About This Trial

The purpose of this clinical study is to assess safety and explore usability and effectiveness of the test product, AAL-FAIOL. This study will be conducted in Central America.

Trial Locations
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Eligibility Criteria
Key Inclusion Criteria: * Able to understand and sign an Informed Consent Form. * Willing and able to attend all scheduled study visits required per protocol. * Diagnosed with bilateral cataracts requiring removal by phacoemulsification. * Preoperative corneal astigmatism equal to or less than 1.50…
Contacts

Alcon Call Center

1-888-451-3937

alcon.medinfo@alcon.com

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