Long Term Follow-up of the VisAbility™ Micro Insert System for Presbyopic Patients

Completed · Not applicable

Conditions studied: Presbyopia

In brief

The objective of this study is to obtain an additional 36 months of safety and effectiveness data from all subjects who were implanted with the VisAbility™ Micro Insert in the VIS-2014 clinical trial.

Key facts

Study ID

NCT03811249

Run by

Refocus Group, Inc.

People needed

287

Starts

2018-12-03

Expected to finish

2021-10-29

Last updated by the study team

2023-11-18

Who can join

Age: 45 and older, up to 60. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects who were implanted with the VisAbility™ Micro Insert in Protocol VIS-2014

You may not qualify if…

• N/A

Where it is running

• Coastal Vision — Orange, California, United States
• Gordon Schanzlin New Vision Institute — San Diego, California, United States
• Aloha Laser Vision — Honolulu, Hawaii, United States
• The Midwest Center for Sight — Des Plaines, Illinois, United States
• Eye Surgeons Of Indiana PC — Indianapolis, Indiana, United States
• Eye Care Institute — Louisville, Kentucky, United States
• Chu Vision Institute — Bloomington, Minnesota, United States
• South Shore Eye Care LLP — Wantagh, New York, United States
• Physicians Protocol — Greensboro, North Carolina, United States
• Comprehensive EyeCare of Central Ohio — Westerville, Ohio, United States
• Bucci Laser Vision — Wilkes-Barre, Pennsylvania, United States
• Key Whitman Eye Center — Dallas, Texas, United States
• Braverman-Terry-Oei-Eye Associates — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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