CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 71 enrolled
Drug / intervention
AcrySof® Toric intraocular lensdevice
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/NCT00762216
NCT00762216N/ACompleted
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Rotational Stability of the AcrySof® Toric

Alcon Research·interventional·Posted Sep 30, 2008·Updated Oct 31, 2012

In Brief

A clinical study evaluating AcrySof® Toric intraocular lens for Cataract. Completed, enrolled 71 participants across 1 site.

Detailed Summary

To assess the rotational stability and the residual refractive cylinder and patient reported outcomes of the AcrySof Toric intraocular lens after unilateral or bilateral implantation.

Study Details

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

Timeline

N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 30, 2008
Enrollment StartMay 1, 2008
Primary CompletionJun 1, 2009
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 17.8 years ago

Interventions

AcrySof® Toric intraocular lensdevice

Implantation of the AcrySof Toric intraocular lens (IOL) into the eye following cataract extraction surgery