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Evaluation of Comfort in Symptomatic Contact Lens Wearers

Not Applicable
Completed
Conditions
Ocular Comfort
Registration Number
NCT04963543
Lead Sponsor
Alcon Research
Brief Summary

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.

Detailed Description

The duration of individual participation is six days.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
17
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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Comfort, collected for each eyeUp to Day 6

A visual analogue scale will be used

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Alcon Investigative Site 6189

🇨🇦

Waterloo, Ontario, Canada

Alcon Investigative Site 6189
🇨🇦Waterloo, Ontario, Canada

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