Lens Wearing Experience and Biocompatibility of a Marketed Multi-Purpose Disinfecting Solution in Silicone Hydrogel and Soft Contact Lens Wearers

Completed · Not applicable

Conditions studied: Refractive Error

In brief

The purpose of this study was to describe mean differences in corneal staining (type and area) for OPTI-FREE PureMoist Multi-Purpose Disinfecting Solution (MPDS) at Day 30 compared to Baseline (Day 0).

Key facts

Study ID

NCT01484938

Run by

Alcon Research

People needed

175

Starts

2011-02-01

Expected to finish

2011-05-01

Last updated by the study team

2012-10-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 years or older
• Soft contact lens wear on a daily wear basis
• Able to wear contact lenses for at least 8 hours
• Generally healthy and have normal ocular health
• Other protocol-defined inclusion criteria may apply

You may not qualify if…

• No use of additional lens cleaners
• No known sensitivities to any ingredient in the test article
• No history of ocular surgery/trauma within the last six months
• 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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