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 |
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.
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.
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
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