CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 222 enrolled
Drug / intervention
VIVITY +3 moredevice
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/NCT04098367
NCT04098367N/ACompleted

A Prospective, Randomized, Controlled, Multi-Center Clinical Investigation of the AcrySof IQ Vivity Extended Vision IOL vs. TECNIS Symfony and AT LARA Extended Depth of Focus IOLs

Alcon Research·interventional·Posted Sep 23, 2019·Updated May 4, 2022

In Brief

A clinical study evaluating VIVITY, SYMFONY, and 2 other interventions for Aphakia. Completed, enrolled 222 participants across 12 sites in 2 countries.

Detailed Summary

The purpose of this study is to compare the visual disturbance profile of an intraocular lens (IOL) using nondiffractive optics, the VIVITY IOL, to two diffractive IOLs in subjects requiring bilateral cataract surgery. IOLs are implantable medical devices intended for long-term use over the lifetime of the cataract patient.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAphakia
CountriesAustralia, New Zealand
Collaborators--

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedSep 23, 2019
Enrollment StartNov 18, 2019
Primary CompletionMay 3, 2021
Study CompletionJul 22, 2021
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 6.8 years ago

Interventions

VIVITYdevice

Extended vision intraocular lens intended for primary implantation for the visual correction of aphakia in adult patients with less than 1.00 diopter of preoperative corneal astigmatism in whom a cataractous lens has been removed by extracapsular cataract extraction

SYMFONYdevice

Extended range of vision intraocular lens indicated for primary implantation for the visual correction of aphakia in adult patients with less than 1.00 diopter of pre-existing corneal astigmatism in whom a cataractous lens has been removed

AT LARAdevice

Extended depth of focus intraocular lens indicated for implantation for the visual correction of aphakia in patients with and without presbyopia in whom a cataractous lens has been removed by extracapsular cataract extraction

Cataract surgeryprocedure

Cataract removal by routine small incision surgery