Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Completed · Not applicable
Conditions studied: Refractive Error
In brief
The purpose of this study is to compare the visual acuity of an investigational silicone hydrogel to a commercially available silicone hydrogel in contact lens wearers.
Key facts
- Study ID
- NCT03095027
- Run by
- Alcon Research
- People needed
- 54
- Starts
- 2017-04-19
- Expected to finish
- 2017-05-15
- Last updated by the study team
- 2019-02-04
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Able to understand and sign an IRB-approved Informed Consent Form;
- Successful wear of spherical soft contact lenses in both eyes for a minimum of 5 days per week and 8 hours per day during the past 3 months:
- Manifest cylinder of ≤ 0.75 diopter (D) in each eye;
- Best corrected visual acuity (BCVA) of 20/25 or better in each eye;
- Other protocol-specified inclusion criteria may apply.
You may not qualify if…
- Any anterior segment infection, inflammation, abnormality or disease (including systemic) that contraindicates contact lens wear, as determined by the Investigator;
- Any use of systemic or ocular medications for which contact lens wear could be contraindicated, as determined by the Investigator;
- History of refractive surgery or plan to have refractive surgery during the study;
- Ocular or intraocular surgery within the previous 12 months or planned during the study;
- Current or history of pathologically dry eye in either eye that, in the opinion of the Investigator, would preclude contact lens wear;
- Any previous or current wear of MYDAY;
- Habitually wearing monovision or multifocal lenses during the last 3 months;
- Routinely sleeping in lenses for at least 1 night per week over the last 3 months prior to enrollment;
- Any use of topical ocular medications and artificial tear or rewetting drops that would require instillation during contact lens wear;
- Other protocol-defined exclusion criteria may apply.
Where it is running
- Alcon Investigative Site — Longwood, Florida, United States
- Alcon Investigative Site — Maitland, Florida, United States
- Alcon Investigative Site — Johns Creek, Georgia, United States
Full record on ClinicalTrials.gov
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