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Completed Not applicable Interventional Results available

Clinical Investigation of the Clareon® Intraocular Lens (IOL)

ClinicalTrials.gov ID: NCT03170154

Public ClinicalTrials.gov record NCT03170154. 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 Oct 21, 2026, 1:37 PM EDT

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

Official title

Clinical Investigation of the Clareon® IOL

Brief summary

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

The objective of this study is to compare visual acuity and adverse event outcomes from the Clareon intraocular lens (IOL) to historical safety and performance endpoint (SPE) rates.

Study identification

NCT ID
NCT03170154
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Alcon Research
Industry
Enrollment
376 participants

Conditions and interventions

Eligibility (public fields only)

Age range
22 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
Jul 25, 2017 (Actual)
Primary completion
Feb 15, 2019 (Actual)
Completion
Feb 15, 2019 (Actual)
Last update posted
Aug 3, 2020

2017 – 2019

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
Alcon Investigative Site Fresno California 93720 —
Alcon Investigative Site Sacramento California 95815 —
Alcon Investigative Site San Leandro California 94578 —
Alcon Investigative Site Deerfield Beach Florida 33064 —
Alcon Investigative Site Orland Park Illinois 60467 —
Alcon Investigative Site Bloomfield Hills Michigan 48302 —
Alcon Investigative Site Kansas City Missouri 64154 —
Alcon Investigative Site New York New York 10013 —
Alcon Investigative Site Poughkeepsie New York 12603 —
Alcon Investigative Site Elizabeth City North Carolina 27909 —
Alcon Investigative Site Southern Pines North Carolina 28387 —
Alcon Investigative Site Florence South Carolina 29501 —
Alcon Investigative Site Ladson South Carolina 29456 —
Alcon Investigative Site Austin Texas 78731 —
Alcon Investigative Site Nacogdoches Texas 75965 —
Alcon Investigative Site Appleton Wisconsin 54914 —

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 NCT03170154, 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 Aug 3, 2020 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03170154 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →