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



Status:Enrolling by invitation
Conditions:Ocular
Therapuetic Areas:Ophthalmology
Healthy:No
Age Range:47 - 62
Updated:1/23/2019
Start Date:December 3, 2018
End Date:July 2021

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A Prospective, Multicenter Clinical Trial of the VisAbility™ Micro Insert System for the Improvement of Near Visual Acuity in Presbyopic Subjects - Long Term Follow-up

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.

VIS-2014-5YR is a multicenter, observational study to evaluate the long-term safety of the
VisAbility™ Micro Inserts in subjects who were implanted with the VisAbility™ Micro Insert in
the VIS-2014 clinical trial. Study subjects will be examined at 36, 48, and 60 months
post-operatively (based on the anniversary of their first VisAbility™ surgery) with no
planned interventions.

Inclusion Criteria:

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

Exclusion Criteria:
We found this trial at
13
sites
Louisville, Kentucky 40206
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Bloomington, Minnesota 55420
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Bloomington, MN
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Dallas, Texas 75204
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Dallas, TX
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Des Plaines, Illinois 60016
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Des Plaines, IL
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Greensboro, North Carolina 27410
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Greensboro, NC
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Honolulu, Hawaii 96814
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Honolulu, HI
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Indianapolis, Indiana 46256
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Indianapolis, IN
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293 South Main Street
Orange, California 92868
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Orange, CA
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San Antonio, Texas 78212
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San Antonio, TX
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San Diego, California 92122
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San Diego, CA
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Wantagh, New York 11793
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Wantagh, NY
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450 Alkyre Run Drive
Westerville, Ohio 43082
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Westerville, OH
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158 Wilkes Barre Township Boulevard
Wilkes-Barre, Pennsylvania 18702
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Wilkes-Barre, PA
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