Cataract lens study checks vision quality after surgery
NCT ID NCT05852470
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how well the Clareon Vivity and Vivity Toric intraocular lenses work in people who already had cataract surgery. Researchers measured vision at different distances in 155 participants. The goal was to confirm the lenses perform as expected and support their use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
155 people
The number who actually took part.
- Started
-
May 2023
- Finished
-
Oct 2023
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Key Inclusion Criteria: * Understand and sign an approved Informed Consent form * Previously implanted in both eyes with Clareon Vivity/Clareon Vivity Toric or Clareon Monofocal/Clareon Toric IOLs for at least 3 months and up to 6 months (90 to 180 days) after second eye implant. * Other protocol-defined inclusion criteria may apply. Key Exclusion Criteria: * History of clinically significant ocular co-morbidities that would affect surgical outcomes based on investigator expert medical opinion. * Subjects who were targeted to monovision defined as ≥ 1.50 Diopter (D) of anisometropia. * Clinically significant PCO (posterior capsule opacification) affecting vision. * Other protocol-defined exclusion criteria may apply.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Aphakia are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Carolina Eyecare Physicians LLC
Mt. Pleasant, South Carolina, 29464, United States
-
Cincinnati Eye Institute
Cincinnati, Ohio, 45242, United States
-
Eye Care Specialists
Kingston, Pennsylvania, 18704, United States
-
Eye Center of Northern Colorado, PC
Fort Collins, Colorado, 80528, United States
-
Grosinger, Spigelman & Grey Eye Surgeons, P.C.
Bloomfield Hills, Michigan, 48302, United States
-
Vance Thompson Vision
Sioux Falls, South Dakota, 57108, United States
-
Wolstan Goldberg Eye Associates
Torrance, California, 90505, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can newer cataract lenses keep vision clear for years?
- New eye lens could let cataract patients ditch glasses
- New lens aims to sharpen vision after cataract surgery
- New lens implant aims to sharpen sight after cataracts
- PanOptix lens safety confirmed years after surgery
- New lens tech aims to sharpen sight after cataracts