Contralateral Claims Study of Clareon Vivity Pro
Status: Recruiting
Location: See all (9) locations...
Intervention Type: Device, Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The purpose of this study is to test new versions of Clareon Vivity Pro intraocular lenses (IOLs) by comparing them to currently marketed IOLs.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 22
Healthy Volunteers: f
View:
• 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.
Locations
Other Locations
Australia
iVision Clinic
RECRUITING
Campsie
Eye Surgery Associates - East Melbourne
RECRUITING
East Melbourne
Peninsula Eye Center
RECRUITING
Mornington
Personaleyes Parramatta
RECRUITING
Sydney
Vision Eye Institute - Chatswood
RECRUITING
Sydney
Wollongong Eye Specialists
RECRUITING
Wollongong
Focus Vision
RECRUITING
Woolloongabba
Philippines
Asian Eye Institute
RECRUITING
Makati City
Peregrine Eye Laser and Institute
RECRUITING
Makati City
Contact Information
Primary
Alcon Call Center
alcon.medinfo@alcon.com
1-888-451-3937
Time Frame
Start Date: 2026-04-28
Estimated Completion Date: 2027-02
Participants
Target number of participants: 231
Treatments
Other: Clareon Vivity Pro IOL / Clareon Vivity IOL (Sub-Study B)
Clareon Vivity Pro IOL implanted in one eye, with Clareon Vivity IOL in the fellow eye, as randomized
Other: Clareon Vivity Pro IOL / TECNIS PureSee IOL (Sub-Study C)
Clareon Vivity Pro IOL implanted in one eye, with TECNIS PureSee IOL in the fellow eye, as randomized
Related Therapeutic Areas
Sponsors
Leads: Alcon Research