Clinical trial
The Purpose of This Research is to Assess Vivity Toric IOL Rotational Stability at the End of Surgery, Post op 1 Day, Post op 1 Week and Post op 4 Weeks. Participants in This Research Study Are 45 Years of Age or Older and Have Planned Implantation in at Least One Eye With an Acrysof IQ Vivity Extended Vision Toric IOL.
NCT05119127 is registered in ClinicalTrials.gov with Kevin Barber as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- The Purpose of This Research is to Assess Vivity Toric IOL Rotational Stability at the End of Surgery, Post op 1 Day, Post op 1 Week and Post op 4 Weeks. Participants in This Research Study Are 45 Years of Age or Older and Have Planned Implantation in at Least One Eye With an Acrysof IQ Vivity Extended Vision Toric IOL.
- Lead sponsor
- Kevin Barber
- Phase
- Not applicable
- Overall status
- Completed
- Start date
- September 30, 2020
- Completion date
- August 19, 2021
- Enrollment
- 35 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.