Loading clinical trials...

A Clinical Comparison of Proclear® 1 Day Multifocal and Clariti® 1 Day Multifocal 3 Add | Clinical Trials | Clareo Health

RECRUITINGNA

A Clinical Comparison of Proclear® 1 Day Multifocal and Clariti® 1 Day Multifocal 3 Add

A Clinical Comparison of Two Soft Multifocal Contact Lenses - Proclear® 1 Day Multifocal and Clariti® 1 Day Multifocal 3 Add

NCT06869044•CooperVision International Limited (CVIL)

View on ClinicalTrials.gov

Summary

The aim of this study is to compare the overall lens satisfaction between two soft multifocal contact lenses.

Detailed Description

The aim of the study is to evaluate the overall lens satisfaction between two soft multifocal contact lenses when compared to each other after 15 minutes of daily wear each.

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•1. They are at least 18 years of age.
•2. They understand their rights as a research subject and are willing and able to sign a Statement of Informed Consent.
•3. They habitually use soft contact lenses (multifocal soft contact lenses, sphere lenses for monovision, sphere lenses for distance vision correction and spectacles for near vision correction,) and have done so for at least the past three months.
•4. They have a minimum reading add of +0.75DS (based on their spectacle refraction)
•5. They have spherical equivalent refractive error between +6.00 to -10.00DS at the corneal plane and refractive astigmatism of no greater than -0.75DC in each eye.
•6. They are able to achieve distance HCVA of +0.10 logMAR or better in each eye.

Exclusion Criteria

•1. They have an ocular disorder which would normally contra-indicate contact lens wear.
•2. They have a systemic disorder which would normally contra-indicate contact lens wear.
•3. They are aphakic.
•4. They have had corneal refractive surgery.
•5. They have any corneal distortion resulting from previous hard or rigid lens wear or have keratoconus.

Locations (1)

University of California, Berkeley, CA

Berkeley, California, United States

Key Dates

Start Date

February 11, 2025

Primary Completion Date

April 30, 2025

Completion Date

April 30, 2025

Last Updated

March 11, 2025

Enrollment

ESTIMATED participants

Conditions

MyopiaHyperopiaPresbyopia

Interventions

omafilcon A lens

DEVICE

Low ADD power somofilcon A lens

DEVICE

Medium ADD power somofilcon A lens

DEVICE

High ADD power somofilcon A lens

DEVICE

Contacts

Jose Vega, OD MSc, PhD

CONTACT

01-925-640-2964 JVega@coopervision.com

Wavefront-guided LASIK Surgery Compared to Ray Tracing-Guided LASIK Surgery

NCT07078799

MyopiaAstigmatism

View study

RECRUITING

IC-8 Apthera IOL New Enrollment Post Approval Study

NCT06060041

CataractPresbyopia+1 more

View study

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: March 11, 2025Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions

A Clinical Comparison of Proclear® 1 Day Multifocal and Clariti® 1 Day Multifocal 3 Add

Inclusion Criteria

Exclusion Criteria

Wavefront-guided LASIK Surgery Compared to Ray Tracing-Guided LASIK Surgery

IC-8 Apthera IOL New Enrollment Post Approval Study

Atropine in the Treatment of Myopia Study in Malaysia

Clinical Study on the Effectiveness of Diverse Segments Defocus Optimization in Spectacle Lenses for Slowing Myopia Progression

China Axial Length Study

Study Comparing Eye Growth Over Time in Children Using Two Myopia Control Lenses