A Study to Evaluate the enVista® Aspire (EA) Intraocular Lens in Subjects Undergoing Cataract Extraction
NCT06333028 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 82
Last updated 2025-05-02
Summary
A Study to Evaluate the enVista® Aspire (EA) intraocular lens in Subjects Undergoing Cataract Extraction
Conditions
- Cataract
Interventions
- DEVICE
-
enVista Aspire EA IOLs
Subjects bilaterally implanted with enVista Aspire EA IOLs
Sponsors & Collaborators
-
Bausch & Lomb Incorporated
lead INDUSTRY
Eligibility
- Min Age
- 22 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-05-30
- Primary Completion
- 2025-03-13
- Completion
- 2025-03-13
- FDA Device
- Yes
Countries
- United States
Study Locations
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