CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 365 enrolled
Drug / intervention
VisAbility Micro Insertdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02374671
NCT02374671N/ACompleted
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A Prospective, Multicenter Clinical Trial of the VisAbility Micro Insert System for Improvement of Near Visual Acuity In Presbyopic Patients

Refocus Group, Inc.·interventional·Posted Mar 2, 2015·Updated Jan 6, 2020

In Brief

A clinical study evaluating VisAbility Micro Insert for Presbyopia. Completed, enrolled 365 participants across 14 sites.

Detailed Summary

The purpose of this study is to evaluate the safety and effectiveness of the VisAbility Micro Insert System for the improvement of near visual acuity in presbyopic patients.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPresbyopia
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedMar 2, 2015
Enrollment StartNov 15, 2014
Primary CompletionApr 13, 2018
TodayJul 2, 2026
Enrollment to primary: 3.4 yearsPosted 11.3 years ago

Interventions

VisAbility Micro Insertdevice

Subjects are implanted with the VisAbility Micro Insert (Model SGP-046) and followed for 24 months.