Evaluation of Comfort of Ocular Lubricants in Symptomatic Contact Lens Wearers
Not Applicable
Completed
- Conditions
- Dry Eye
- Registration Number
- NCT05741216
- Lead Sponsor
- Alcon Research
- Brief Summary
The purpose of this study is to evaluate the ocular comfort of 3 ocular lubricants and a comparator.
- Detailed Description
The expected duration of subject participation is at least 7 days. This study will be conducted in Australia and Canada.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 36
Inclusion Criteria
- Is able to understand and sign an approved information consent letter;
- Habitually wears daily disposable soft contact lenses in both eyes
- Uses rewetting drops on a regular basis;
- 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 specified exclusion criteria may apply.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Ocular comfort Up to Day 5 Comfort will be rated using a visual analog scale (0-100) from 0-100, where 0=poor and 100=excellent.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (3)
School of Optometry and Vision
🇦🇺Sydney, New South Wales, Australia
Deakin Collaborative Eye Care Clinic, Deakin University
🇦🇺Waurn Ponds, Victoria, Australia
School of Optometry and Vision Science, University of Waterloo
🇨🇦Waterloo, Ontario, Canada
School of Optometry and Vision🇦🇺Sydney, New South Wales, Australia