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Completed Not applicable Interventional Results available

Evaluation of Product Performance of a New Silicone Hydrogel Multifocal Contact Lens

ClinicalTrials.gov ID: NCT05660577

Public ClinicalTrials.gov record NCT05660577. 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, 11:08 AM EDT

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

Official title

A Study to Evaluate the Product Performance of a New Silicone Hydrogel Multifocal Contact Lens

Brief summary

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

The objective of this study is to evaluate the product performance of a new silicone hydrogel daily disposable multifocal contact lens, the Bausch + Lomb (kalifilcon A) Daily Disposable Multifocal Contact Lens, when worn by current soft contact lens wearers on a daily disposable wear basis

Study identification

NCT ID
NCT05660577
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Bausch & Lomb Incorporated
Industry
Enrollment
301 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 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
Nov 6, 2022
Primary completion
Jan 15, 2023
Completion
Jan 15, 2023
Last update posted
Apr 8, 2024

2022 – 2023

United States locations

U.S. sites
20
U.S. states
12
U.S. cities
19
Facility City State ZIP Site status
Eric White OD Inc San Diego California 92123
Lee & Woo Optometry San Francisco California 94112
Chester T Roe III MD Prof LLC Denver Colorado 80246
Pearle Vision Jacksonville Florida 32246
Eola Eyes Orlando Florida 32803
Vision Health Institute Orlando Florida 32803
Golden Vision Sarasota Florida 34237
The Eyecare Studio, LLC Decatur Georgia 30035
Family Eyecare Center Leavenworth Kansas 66048
Kannarr EyeCare Pittsburg Kansas 66762
Casco Bay EyeCare Portland Maine 04101
Cornea and Contact Lens Institute of Minnesota Edina Minnesota 55436
Koetting Associates St Louis Missouri 63144
Spectrum Eyecare Jamestown New York 14701
Saccco Eye Group Vestal New York 13850
Oculus Research Raleigh North Carolina 27603
CORE, Inc. Shelby North Carolina 28150
West Bay Eye Associates Warwick Rhode Island 02888
Total Eye Care, PA Memphis Tennessee 38119
Optometric Physicians of Middle Tennessee Nashville Tennessee 37205

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 NCT05660577, 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 Apr 8, 2024 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05660577 live on ClinicalTrials.gov.

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