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OpenTrials
Completed

NCT Number: NCT06400914

Clinical Evaluation of Biomedics Monthly Sphere and Avaira Vitality Sphere

The aim of this study is to compare the short-term clinical performance of two sphere contact lenses.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Consultorio Optométrico Queretaro

Mexico City, 06760, Mexico

About this study

The aim of this study is to evaluate the short-term clinical performance of two different sphere contact lenses 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

  • Is at least 18 years of age and has full legal capacity to volunteer.
  • Has read and signed an information consent letter.
  • Self-reports having a full eye examination in the previous two years.
  • Anticipates being able to wear the study lenses for the required time of the study.
  • Is willing and able to follow instructions and maintain the appointment schedule.
  • Has refractive astigmatism no higher than -0.75 DC.
  • Can be fit with the available lens parameters (sphere +6.00 to -10.00D).
  • Can achieve binocular distance vision of at least 20/30 Snellen (logMAR 0.18) with the study contact lenses.

Exclusion criteria

  • Is participating in any concurrent clinical or research study.
  • Has any known active ocular disease and/or infection that contraindicates contact lens wear.
  • Has a systemic condition that in the opinion of the investigator may affect a study outcome variable.
  • Is using any systemic or topical medications that in the opinion of the investigator may affect contact lens wear or a study outcome variable.
  • Has known sensitivity to the diagnostic sodium fluorescein used in the study.
  • Self-reports as pregnant, lactating or planning a pregnancy at the time of enrolment.
  • Has undergone refractive error surgery or intraocular surgery.

Treatment and study plan

Lens A (ocufilcon D)

Device

15 minutes of daily wear.

Lens B (fanfilcon A)

Device

15 minutes of daily wear.

Primary outcomes

  1. Lens Fit Acceptance Ratings

    Time frame: At the end of 15 Minutes of wear

    Overall lens fit acceptance was measured on a scale from 0-4 (0=Should not be worn and 4= Perfect)

Sponsors and collaborators

Lead sponsor

CooperVision, Inc.

Industry

Collaborators

  • Centre for Ocular Research & Education, Canada

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
May 6, 2024
Registry last updated
Aug 15, 2025

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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