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The purpose of this study is to evaluate the safety and effectiveness of an investigational IOL.
Full description
Eligible subjects will receive the investigational IOL in one eye and be followed at 1 day, 1 week, 1 month, 3 months, 6 months, 12 months, 18 months, 24 months and 36 months post-operation.
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Inclusion and exclusion criteria
Key Inclusion Criteria:
Key Exclusion Criteria:
Primary purpose
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Interventional model
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170 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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