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Recruiting

NCT Number: NCT07444658

Performance of Two Daily Disposable Multifocal Contact Lenses

This study will compare the performance of two daily disposable multifocal soft contact lenses.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of California, Berkeley

Berkeley, California, 94720, United States

Location status: Recruiting

Location contact

Meng C Lin, OD, PhD

CONTACT

510-643-9252

About this study

This is a double-masked, randomized, crossover, 1-week, real world dispensing study, where participants will wear two designs of daily disposable soft multifocal contact lenses for 5-7 days 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 participant 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, or sphere lenses for distance vision correction and spectacles for near vision correction,) and have worn lenses at least 3 days a week for at least the past six 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 HCHL visual acuity 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

Lens A (kalfilcon A)

Device

Daily disposable, soft contact lenses worn for one week

Lens B (stenfilcon A)

Device

Daily disposable, soft contact lenses worn for one week

Primary outcomes

  1. Subjective Visual Acuity

    Time frame: Through study completion, approximately 4 hours

    High contrast high luminance (HCHL) distance binocular visual acuity (logMAR)

Study contacts

Contact information is provided by the study sponsor or research team.

Jose A Vega, OD,MSc,PhD

CONTACT

[email protected]

9256213761

Sponsors and collaborators

Lead sponsor

CooperVision International Limited (CVIL)

Industry

Collaborators

  • University of California, Berkeley

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Mar 3, 2026
Registry last updated
Apr 8, 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.

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