Clinical Comparison of Two Daily Disposable Soft Contact Lenses
Completed · Not applicable
Conditions studied: Myopia, Refractive Errors
In brief
The purpose of this study is to evaluate the overall performance of investigational contact lenses (DD T2) when compared to clariti® 1 day contact lenses.
Key facts
- Study ID
- NCT03518008
- Run by
- Alcon Research
- People needed
- 22
- Starts
- 2018-05-23
- Expected to finish
- 2018-06-11
- Last updated by the study team
- 2019-04-03
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Understand and sign an Informed Consent Form;
- Successful wear of daily disposable 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;
- Best-corrected visual acuity (BCVA) 20/25 or better in each eye;
- Willing to stop wearing habitual contact lenses for the duration of study participation;
- Other protocol-specified inclusion criteria may apply.
You may not qualify if…
- Anterior segment infection, inflammation, or abnormality or disease that contraindicates contact lens wear, as determined by the Investigator;
- Use of systemic or ocular medications for which contact lens wear could be contraindicated, as determined by the Investigator;
- Refractive, ocular, or intraocular surgery, as specified in the protocol;
- Eye condition or injury, as specified in the protocol;
- Current or history of intolerance, hypersensitivity, or allergy to any component of the study products;
- Wearing habitual contact lenses in an extended wear modality (routinely sleeping in lenses for at least 1 night per week) over the last 3 months prior to enrollment;
- Use of topical ocular medications and artificial tear or rewetting drops requiring instillation during contact lens wear;
- Currently wearing clariti® 1 day contact lenses;
- Habitually wearing monovision or multifocal lenses during the last 3 months;
- Other protocol-specified exclusion criteria may apply.
Where it is running
- Alcon Investigative Site — Maitland, Florida, United States
Full record on ClinicalTrials.gov
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