Expired Study
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Fort Worth, Texas 76134


Purpose:

The purpose of this study is to evaluate Clear Care® Plus compared to PeroxiClear™ for mean residual peroxide in used lens cases collected at Day 30.


Study summary:

The subject will wear habitual lenses on a daily wear basis and use the assigned test solution for daily lens care.


Criteria:

Inclusion Criteria: - Sign informed consent form; - Adapted, 2-week/monthly replacement silicone hydrogel contact lens wearers (at least 2 months); - Willing to wear study lenses daily wear only on a daily basis (7 days per week and at least 4 hours per day) and attend all study visits; - Symptoms of contact lens related dryness as defined by the Symptomatic Pre-Screening Questionnaire; - Other protocol-specified inclusion criteria may apply. Exclusion Criteria: - Current hydrogen peroxide-based solution user; - Routinely sleeps in lenses at least 1 night per week over the last 3 months prior to enrollment; - Ocular anterior segment infection, inflammation, abnormality, or active disease that would contraindicate contact lens wear; - Any systemic diseases that may affect the eye or be exacerbated by use of contact lenses or contact lens solutions or which could prevent wearing lenses at least 4 hours per day; - Use of systemic or ocular medications for which contact lens wear could be contraindicated; - Monocular (only 1 eye with functional vision) or fit with only 1 lens; - History of herpetic keratitis, ocular surgery, or irregular cornea; - Other protocol-specified exclusion criteria may apply.


NCT ID:

NCT02413333


Primary Contact:

Study Director
Maria Sangemino
Alcon Research


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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