Clareon TruPlus Single-Arm Study
Status: Recruiting
Location: See all (5) locations...
Intervention Type: Device, Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The purpose of this research study is to generate safety and performance data for Clareon TruPlus Monofocal Intraocular Lenses (IOLs). IOLs are medical devices that are implanted in the eye during cataract surgery to restore clear vision after the cloudy natural lens has been removed. IOLs are intended to remain in the eyes for the duration of the patient's lifetime.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 22
Healthy Volunteers: f
View:
• Diagnosed with bilateral cataracts and planned bilateral cataract extraction by routine phacoemulsification.
• Potential postoperative BCDVA of 0.2 logMAR or better in each eye in the expert medical opinion of the investigator.
• Astigmatism suitable for correction with available toric IOL models.
• Other protocol-specified inclusion criteria may apply.
Locations
United States
Arizona
Eye Doctors of Arizona
RECRUITING
Phoenix
Ohio
Cleveland Eye Clinic
RECRUITING
Brecksville
South Carolina
Carolina Eyecare Physicians LLC
RECRUITING
Mt. Pleasant
Texas
Berkeley Eye Center
RECRUITING
Sugar Land
Utah
The Eye Institute of Utah
RECRUITING
Salt Lake City
Contact Information
Primary
Alcon Call Center
alcon.medinfo@alcon.com
1-888-451-3937
Time Frame
Start Date: 2026-05-26
Estimated Completion Date: 2028-06
Participants
Target number of participants: 122
Treatments
Experimental: Clareon TruPlus Monofocal IOL
Implantation with the Clareon TruPlus Monofocal IOL (Non-Toric or Toric) following removal of the clouded natural lens using phacoemulsification
Related Therapeutic Areas
Sponsors
Leads: Alcon Research