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Terminated Phase 3 Interventional

A Prospective Multicenter Clinical Study to Evaluate the Safety and Effectiveness of the Synchrony Dual Optic Intraocular Lens in Patients Undergoing Cataract Extraction

ClinicalTrials.gov ID: NCT00425464

Public ClinicalTrials.gov record NCT00425464. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 5:23 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the study is to determine if the Synchrony Dual Optic Accommodating Intraocular Lens can be used safely and effectively in post cataract extraction subjects

Study identification

NCT ID
NCT00425464
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Abbott Medical Optics
Industry
Enrollment
410 participants

Conditions and interventions

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2005
Primary completion
Mar 31, 2013
Completion
Mar 31, 2013
Last update posted
Sep 18, 2013

2005 – 2013

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Harvard Eye Associates Laguna Hills California 92653
Long Beach Laser Center Los Alamitos California 90720
Altos Eye Physicians Los Altos California 94024
Grutzmacher & Lewis Sacramento California 95815
Davidorf Eye Group West Hills California 91307
Glaucoma Consultants of Colorado Parker Colorado 80134
Katzen Eye Care and Laser Center Boynton Beach Florida 33426
EyeSight Hawaii Honolulu Hawaii 96817
The Midwest Center for Sight Des Plaines Illinois 60016
NorthShore University HealthSystem Glenview Illinois 60026
Wallace Eye Surgery Alexandria Louisiana 71303
Chu Vision Institute Bloomington Minnesota
Associated Eye Care Stillwater Minnesota 55082
Pepose Vision Institute Chesterfield Missouri 63017
Nevada Eye Care Las Vegas Nevada 89129
Drs. Fine, Hoffman & Packer Eugene Oregon 97401
Alkek Eye Center Houston Texas 77030
University of Utah Hospitals and Clinics Salt Lake City Utah 84132
Northwest Eye Surgeons Seattle Washington 98133
Davis Duehr Dean Madison Wisconsin 53715

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00425464, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 18, 2013 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00425464 live on ClinicalTrials.gov.

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