Post Approval Study to Evaluate the Trulign™ Toric Posterior Chamber IOL
NCT02394379 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 600
Last updated 2019-11-13
Summary
To evaluate the incidence of IOL vaulting (ie, position change) of the Trulign™ Toric IOL following cataract surgery.
Conditions
- Cataract
Interventions
- DEVICE
-
Trulign™ Toric IOL
Trulign™ Toric Posterior Chamber IOL is a modified plate haptic lens
Sponsors & Collaborators
-
Bausch Health Americas, Inc.
collaborator INDUSTRY -
Bausch & Lomb Incorporated
lead INDUSTRY
Principal Investigators
-
Anya Loncaric · Valeant Pharmaceuticals NA / Bausch & Lomb
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-03-19
- Primary Completion
- 2019-08-05
- Completion
- 2019-08-05
Countries
- United States
Study Locations
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