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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 Oct 20, 2026, 6:09 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 7, 2022 (Actual)
Primary completion
Jan 16, 2023 (Actual)
Completion
Jan 16, 2023 (Actual)
Last update posted
Apr 9, 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 9, 2024 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05660577 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →