NCT04963543
Completed
Not Applicable
Evaluation of Comfort in Symptomatic Contact Lens Wearers
ConditionsOcular Comfort
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Ocular Comfort
- Sponsor
- Alcon Research
- Enrollment
- 17
- Locations
- 1
- Primary Endpoint
- Comfort, collected for each eye
- Status
- Completed
- Last Updated
- 4 years ago
Overview
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.
Investigators
Eligibility Criteria
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.
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.
Outcomes
Primary Outcomes
Comfort, collected for each eye
Time Frame: Up to Day 6
A visual analogue scale will be used
Study Sites (1)
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