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
Name Time Method Comfort, collected for each eye Up to Day 6 A visual analogue scale will be used
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Alcon Investigative Site 6189
🇨🇦Waterloo, Ontario, Canada
Alcon Investigative Site 6189🇨🇦Waterloo, Ontario, Canada