IC-8 Apthera IOL New Enrollment Post Approval Study
NCT06060041 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 435
Last updated 2026-01-12
Summary
The purpose of this study is to verify the post-market safety of the IC-8 Apthera IOL after the treatment of posterior capsular opacification (PCO), an expected complication related to IC-8 Apthera IOL implantation.
Conditions
- Cataract
- Presbyopia
- Posterior Capsule Opacification
Sponsors & Collaborators
-
Bausch & Lomb Incorporated
lead INDUSTRY
Eligibility
- Min Age
- 22 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-09-08
- Primary Completion
- 2027-09-30
- Completion
- 2027-09-30
Countries
- United States
Study Locations
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