NCT04128514

Spectacle Independence and Overall Satisfaction With AcrySof® Panoptix® Toric Intraocular Lens

Spectacle Independence and Overall Satisfaction With Bilateral Implantation of the AcrySof® Panoptix® Toric Intraocular Lens

• Status: Terminated
• Phase: —
• Study type: Observational
• Enrollment: 15 (actual)
• Sponsor: Eye Center of North Florida · Academic / Other
• Sex: All
• Age: 40 Years
• Healthy volunteers: Accepted

Summary

The study was designed to assess the spectacle independence and satisfaction of patients receiving the AcrySof® Panoptix® Toric intraocular lens (IOL) after uneventful cataract surgery.

Detailed description

This study is a single-arm unmasked clinical evaluation study of spectacle independence after successful bilateral cataract surgery. Subjects will be assessed pre-operatively, operatively and at 1 day, 1 month and 3 months post-operatively. Clinical evaluations will include administration of a spectacle independence and a quality of life questionnaire, as well as measurement of bilateral visual acuity and manifest refraction.

Conditions

• Cataract

Interventions

Type	Name	Description
DEVICE	Panoptix Toric	Cataract surgery and IOL implantation

Timeline

• Start date: 2019-10-11
• Primary completion: 2022-03-10
• Completion: 2022-03-10
• First posted: 2019-10-16
• Last updated: 2022-04-01

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study