Skip to main content
OpenTrials
Completed

NCT Number: NCT06869044

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

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

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of California, Berkeley, CA

Berkeley, California, 94720, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • They are at least 18 years of age.
  • They understand their rights as a research subject and are willing and able to sign a Statement of Informed Consent.
  • 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.
  • They have a minimum reading add of +0.75DS (based on their spectacle refraction)
  • 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.
  • They are able to achieve distance HCVA of +0.10 logMAR or better in each eye.

Exclusion criteria

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

Treatment and study plan

omafilcon A lens

Device

Participants will be randomized to wear omafilcon A lens for 15 minutes.

Low ADD power somofilcon A lens

Device

Participants will be randomized to wear low ADD power somofilcon A lens for 15 minutes.

Medium ADD power somofilcon A lens

Device

Participants will be randomized to wear medium ADD power somofilcon A lens for 15 minutes.

High ADD power somofilcon A lens

Device

Participants will be randomized to wear high ADD power somofilcon A lens for 15 minutes.

Primary outcomes

  1. Overall lens satisfaction

    Time frame: At the end of 15 minutes wear

    Overall Impression recorded on a visual analog scale of 0 to 100 where (0=Extremely poor. Unmanageable. Cannot use lenses, 100=Excellent. Highly impressed with these lenses overall.)

Sponsors and collaborators

Lead sponsor

CooperVision International Limited (CVIL)

Industry

Collaborators

  • University of California, Berkeley

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Mar 11, 2025
Registry last updated
Apr 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.