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OpenTrials
Completed

NCT Number: NCT04963543

Evaluation of Comfort in Symptomatic Contact Lens Wearers

The purpose of this study is to evaluate the comfort of an ocular lubricant in symptomatic contact lens wearers. This study will be conducted in Canada.

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Key information

Conditions

Ocular Comfort

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Alcon Investigative Site 6189

Waterloo, Ontario, N2L 3G1, Canada

About this study

The duration of individual participation is six days.

Who can participate

Healthy volunteers accepted: No

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

Key Inclusion Criteria:

  • Is able to understand and sign an approved information consent letter;
  • Habitually wears daily disposable soft contact lenses in both eyes;
  • Is able to achieve 20/40 or better monocular VA with habitual contact lenses;
  • Has a pair of spectacles for vision correction.
  • Other protocol-defined inclusion criteria may apply.

Key Exclusion Criteria:

  • Routinely sleeps in habitual contact lenses;
  • Has any known active ocular disease and/or infection;
  • Is pregnant or lactating;
  • Other protocol-defined exclusion criteria may apply.

Treatment and study plan

FID123238

Other

Lubricant applied to the ocular surface

Primary outcomes

  1. Comfort, collected for each eye

    Time frame: Up to Day 6

    A visual analogue scale will be used

Sponsors and collaborators

Lead sponsor

Alcon Research

Industry

Registry information

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Jul 15, 2021
Registry last updated
Nov 3, 2021

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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