RecruitingNot ApplicableNCT06869044

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


Sponsor

CooperVision International Limited (CVIL)

Enrollment

66 participants

Start Date

Feb 11, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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


Eligibility

Min Age: 18 Years

Inclusion Criteria6

  • 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 Criteria5

  • 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.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DEVICEomafilcon A lens

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

DEVICELow ADD power somofilcon A lens

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

DEVICEMedium ADD power somofilcon A lens

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

DEVICEHigh ADD power somofilcon A lens

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


Locations(1)

University of California, Berkeley, CA

Berkeley, California, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06869044


Related Trials