New lens tech aims to sharpen sight after cataracts
NCT ID NCT07484191
First seen Jun 27, 2026 · Last updated Aug 07, 2026 · Updated 5 times
Summary
This study tests new versions of Clareon Vivity Pro intraocular lenses (IOLs) to see if they improve vision better than current lenses. About 231 adults with cataracts in both eyes will receive one new lens and one current lens to compare results. The main goal is to measure how well participants see at arm's length (66 cm) in bright light.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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165 people
The number who actually took part.
- Started
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Apr 2026
- Expected to finish
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Feb 2027
An estimate. End dates often move.
- Lead sponsor
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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
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22 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Key Inclusion Criteria: * Cataracts in both eyes. * Preoperative corneal astigmatism of less than 1.00 diopter (D) in each eye. * Potential postoperative best corrected visual acuity (BCDVA) of 0.2 logMAR or better in each eye in the expert medical opinion of the investigator. * Other protocol-defined inclusion criteria may apply. Key Exclusion Criteria: * Desires monovision correction. * Predicted post-operative residual astigmatism of more than 1D in either eye. * Any ocular or systemic co-morbidity that, in the investigator's medical opinion, may confound the results of this study, prohibit the completion of the study assessments, or increase the risk for the subject. * Other protocol-defined exclusion criteria may apply.
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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
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Eye Surgery Associates - East Melbourne
East Melbourne, Victoria, 3002, Australia
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Focus Vision
Woolloongabba, Queensland, 4102, Australia
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Peninsula Eye Center
Mornington, Victoria, 3931, Australia
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Personaleyes Parramatta
Sydney, New South Wales, 2150, Australia
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Vision Eye Institute - Chatswood
Sydney, New South Wales, 2067, Australia
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Wollongong Eye Specialists
Wollongong, New South Wales, 2500, Australia
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iVision Clinic
Campsie, New South Wales, 2194, Australia
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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