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Clinical Trial Summary

Purpose is to study the clinical outcomes of Clareon Vivity and Clareon Vivity Toric intraocular lens (IOL) implants in patients who are planning to have cataract surgery in both eyes with a mini-monovision approach.


Clinical Trial Description

A "mini-monovision" approach is one in which the dominant eye is corrected for distance vision while the non-dominant eye is corrected with a small amount of nearsightedness (-0.5 diopters). This approach can have the benefit of increasing ability to see over a broad range of vision without glasses. The Clareon Vivity and Vivity Toric lenses have been approved by the U.S. Food and Drug Administration (FDA) for visual correction of aphakia in adult patients following cataract surgery. It has lens technology that provides an extended depth of focus (more range of clear vision for distance, intermediate and near vision) compared to a standard monofocal (single focus) lens. None of the procedures in this study are experimental. However, the study is seeking additional information on clinical outcomes of the mini-monovision approach specifically using the Clareon Vivity and Vivity Toric lenses. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05821101
Study type Interventional
Source Palo Alto Medical Foundation
Contact Sharon De Paz, LVN
Phone (650) 853-2424
Email sharontanya.depaz@sutterhealth.org
Status Recruiting
Phase N/A
Start date April 6, 2023
Completion date December 2024

See also
  Status Clinical Trial Phase
Completed NCT04005651 - Safety and Efficacy of a Trifocal Intraocular Lens (IOL) POD L GF in Comparison With a Multifocal and a Monofocal IOL N/A
Recruiting NCT06363448 - Yamani Technique Versus Proline Mesh for Intraocular Lens Scleral Fixation in Aphakia N/A