Evaluation of the Symfony With Optiblue Intraocular Lens Compared to The Vivity IOL Under Mesopic Conditions

Status: Completed
Location: See all (2) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

The purpose of this study is to evaluate the visual outcomes of the Symfony lens and the Vivity lens under mesopic lighting conditions in adult patients undergoing routine cataract surgery. Participants will be asked to read a visual acuity chart at different distances in dim light.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Healthy Volunteers: f
View:

• Subject is undergoing bilateral lens extraction with implantation of an EDOF IOL with a target refraction of plano OU.

• Gender: Males and Females.

• Age: 50 years and older.

• Willing and able to provide written informed consent for participation in the study

• Willing and able to comply with scheduled visits and other study procedures.

• Scheduled to undergo standard cataract surgery in both eyes, with 1 to 30 days between surgeries.

• Potential postoperative visual acuity of 0.2 logMAR (20/32 Snellen) or better in both eyes.

Locations
United States
Florida
Center for Sight
Sarasota
South Carolina
Carolina Eyecare Physicians, LLC
Mt. Pleasant
Time Frame
Start Date: 2023-12-01
Completion Date: 2024-10-30
Participants
Target number of participants: 64
Treatments
Active_comparator: Symfony IOL
The Symfony IOL is a lens designed to provide high quality vision up tp 26 inches reducing the need for glasses after routine cataract surgery in patients with or without astigmatism.
Active_comparator: Vivity IOL
The Vivity IOL is a lens that provides extended range of vision ranging from distance to near reducing the need for glasses after routine cataract surgery in patients with or without astigmatism.
Related Therapeutic Areas
Sponsors
Leads: Carolina Eyecare Physicians, LLC
Collaborators: Science in Vision

This content was sourced from clinicaltrials.gov