Expired Study
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Fort Worth, Texas 76134


Purpose:

Evaluate daily disposable lenses inserted out of the blister package versus daily disposable lenses inserted after a pre-soak in Multi-purpose solution FID 107027


Criteria:

Inclusion Criteria: - No requirement as to subject sex, race, occupation or reason for wearing contact lenses. - Subjects visual acuity must be correctable to 20/30 (Snellen) or better in each eye at distance with contact lenses to enter the study - Subjects must be successfully wearing hydrogel or silicone hydrogel contact lenses prior to study Exclusion Criteria: - History of hypersensitivity to any components of the solution - Evidence or history of keratitis - One functional eye or a monofit lens - Active acute blepharitis, corneal infections or iritis. - Any abnormal slit-lamp finding at visit 1 of each study period. - Significant corneal staining at visit 1 of each study period.


NCT ID:

NCT00733291


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Fort Worth, Texas 76134
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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