CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 30 enrolled
Drug / intervention
RESTOR IOL Model SA60D3device
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/NCT00759096
NCT00759096N/ACompleted
CompareCT.gov

Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL

Alcon Research·interventional·Posted Sep 25, 2008·Updated Dec 5, 2023

In Brief

A clinical study evaluating RESTOR IOL Model SA60D3 for Visual Acuity. Completed, enrolled 30 participants across 1 site.

Detailed Summary

The purpose of this study is to assess uniocular and binocular unaided distance, intermediate, and near VA; contrast sensitivity, accommodation amplitude, stereopsis, glare testing, ocular aberrations and the clinical satisfaction assessment after bilateral implant of the Restor IOL.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsVisual Acuity
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 25, 2008
Enrollment StartMay 1, 2007
Primary CompletionJul 1, 2008
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 17.8 years ago

Interventions

RESTOR IOL Model SA60D3device

Implanted into the study eye following cataract extraction surgery