A Multi-Center Investigation of Patient Acceptability of OPTI-FREE RepleniSH® Multi-Purpose Disinfecting Solution (MPDS)

Completed · Not applicable

Conditions studied: Myopia

In brief

The purpose of this study was to demonstrate that current successful fulltime daily wear soft contact lens wearers using competitive multi-purpose solutions will note improved comfort when using OPTI-FREE RepleniSH®.

Key facts

Study ID

NCT00772707

Run by

Alcon Research

People needed

114

Starts

2008-09-01

Expected to finish

2008-10-01

Last updated by the study team

2012-09-07

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants must be between 18 and 65 years of age.
• Must wear daily wear soft contact lenses a minimum of 8 hours per day,7 days a week.
• Must be wearing a planned replacement soft lens in a 2 week or monthly replacement modality.
• Must be using either COMPLETE Multi-Purpose Solution (MPS) Easy Rub or ReNu MultiPlus brand solution for at least 30 continuous days prior to enrollment.
• Must be free of any contact lens-related symptoms with regard to comfort and vision throughout their wearing hours prior to enrollment, with the exception of end-of-day dryness not limiting all day wear.
• Must have best corrected distance visual acuity, with contact lenses, of 20/30 or better in each eye.
• Must be willing to maintain pre-enrollment systemic medication regimens during the study.
• Must be willing to not use any topical medications or rewetting drops during the 30 day clinical trial duration.
• Other protocol-defined inclusion criteria may apply.

You may not qualify if…

• Has used any topical medication or rewetting drops for 7 days prior to enrollment.
• Achieves best visual correction by monovision.
• Has modified their systemic medications within 30 days prior to enrollment.
• Has switched brands of cosmetics during the 30 days prior to the study.
• Has a history of allergy to any study product ingredients.
• Is unwilling or unable to meet the study visit timeline.
• Has any active corneal, eyelid or other anterior segment inflammation or infection, which, in the opinion of the Investigator, would adversely affect successful contact lens wear.
• Other protocol-defined exclusion criteria may apply.

Where it is running

• Alcon Call Center for Trial Locations — Fort Worth, Texas, United States

Full record on ClinicalTrials.gov

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