Effect of FID 114675A on Lens Wettability
Completed · Not applicable
Conditions studied: Contact Lens Wettability
In brief
The purpose of this study is to evaluate lens wettability of contact lenses when used with an investigational multi-purpose disinfecting solution.
Key facts
- Study ID
- NCT01342107
- Run by
- Alcon Research
- People needed
- 66
- Starts
- 2010-12-01
- Expected to finish
- 2011-02-01
- Last updated by the study team
- 2012-04-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 18 years or age or older with normal eyes, other than correction for refractive error.
- At least 5 days successful daily wear (minimum 8 hours per day) of PureVision®, Acuvue® Oasys™, or Acuvue® 2 contact lenses prior to Visit 1
- Vision correctable to 20/30 (Snellen) or better in each eye at distance with lenses at Visit 1 (Day 0 - Baseline).
- Grade 0 or Grade 1 wettability in both eyes after at least 15 minutes of lens wear at Visit 1 (Day 0 - Baseline).
- Other protocol-defined inclusion criteria may apply.
You may not qualify if…
- Any ocular or systemic medical condition that may, in the opinion of the investigator, preclude safe administration of the test articles or affect the results of the study.
- Need to wear contact lenses on an extended wear basis (i.e., overnight) during the study.
- Use of products other than a multi-purpose solution or hydrogen peroxide solution, including daily and enzyme cleaners and saline rinses, for lens care at least 7 days prior to Visit 1 (Day 0 - Baseline).
- Use of over-the-counter (OTC) or prescribed topical ocular medications within 7 days prior to Visit 1. Use of lens rewetting drops is acceptable.
- History or current ocular infections or ocular inflammatory events.
- Ocular surgery within the past year.
- Participation in any investigational study within the past 30 days.
- Other protocol-defined exclusion criteria may apply.
Where it is running
- Contact Alcon Call Center for Trial Locations — Fort Worth, Texas, United States
Full record on ClinicalTrials.gov
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