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OpenTrials
Completed

NCT Number: NCT04296877

Evaluation of Wear Experience With a Daily Disposable Contact Lens

To evaluate the wear experience of current two-week contact lens wearers after they have been fit into a daily disposable contact lens. This is a single arm, non-comparative study.

Completed

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Key information

Conditions

Contact Lens

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Ohio State University College of Optometry

Columbus, Ohio, 43210, United States

About this study

This is a single arm, non-comparative study. All participants were habitual lens wearers of the same brand of lenses, and were re-fit with the study lenses.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Must be current Acuvue® Oasys® spherical contact lens wearers.
  • Distance visual acuity of 20/25 or better with current contact lenses.
  • Good general health (defined by medication use that has not changed within the last month and the absence of medical conditions or treatments that are deemed confounding to the data as determined by the PI).
  • Ability to give informed consent.
  • Willing to spend time for the study, which includes attending two study visits and wearing contact lenses on days between study visits.
  • Either gender.
  • Any racial or ethnic origin.

Exclusion criteria

  • No current ocular inflammation or infection.
  • Not currently pregnant or lactating.

Treatment and study plan

daily disposable contact lens

Device

Soft, daily disposable spherical contact lens used to correct distance vision.

Primary outcomes

  1. Contact Lens Dry Eye Questionnaire (CLDEQ-8) Survey

    Time frame: 2 weeks

    Participants complete the Contact Lens Dry Eye Questionnaire (CLDEQ-8) survey. This is an 8 question survey assesses symptoms while wearing contact lenses with possible scores from 0 (no symptoms) to 37 (maximum symptoms). Higher scores indicate worsening symptoms of dry eye while wearing lenses.

Sponsors and collaborators

Lead sponsor

Ohio State University

Other

Collaborators

  • Alcon Research

Registry information

Official study title

Evaluation of Wear Experience With PRECISION1® Contact Lenses in Previous Acuvue® Oasys® Lens Wearers

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Mar 5, 2020
Registry last updated
Mar 7, 2023

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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