CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 151 enrolled
Drug / intervention
AcuFocus Corneal Inlay ACI 7000PDTdevice
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/NCT01352442
NCT01352442N/ACompleted
CompareCT.gov

A Prospective Multicenter Clinical Trial to Evaluate the Safety and Effectiveness of the AcuFocus Corneal Inlay ACI 7000PDT Implanted Intrastromally for Modified Monovision in Presbyopic Subjects

AcuFocus, Inc.·interventional·Posted May 11, 2011·Updated Mar 28, 2017

In Brief

A clinical study evaluating AcuFocus Corneal Inlay ACI 7000PDT for Presbyopia. Completed, enrolled 151 participants across 11 sites in 10 countries.

Detailed Summary

The purpose of this study is to determine if the AcuFocus Corneal Inlay ACI 7000PDT will provide an effective method of for the correction of presbyopia in patients who have normal distance vision but need correction such as glasses or contact lenses to see clearly at near.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPresbyopia
CountriesAustralia, Austria, France, Japan, Netherlands, New Zealand, Philippines, Singapore, Spain, Turkey (Türkiye)
Collaborators--

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedMay 11, 2011
Enrollment StartMay 1, 2011
Primary CompletionMar 1, 2014
TodayJul 2, 2026
Enrollment to primary: 2.8 yearsPosted 15.1 years ago

Interventions

AcuFocus Corneal Inlay ACI 7000PDTdevice

corneal inlay