Status:

COMPLETED

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

Lead Sponsor:

Alcon Research

Conditions:

Refractive Error

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

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)...

Eligibility Criteria

Inclusion

  • 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

Exclusion

  • 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

Key Trial Info

Start Date :

February 1 2011

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 1 2011

Estimated Enrollment :

175 Patients enrolled

Trial Details

Trial ID

NCT01484938

Start Date

February 1 2011

End Date

May 1 2011

Last Update

October 10 2012

Active Locations (1)

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1

Contact Alcon Call Center for Trial Locations

Fort Worth, Texas, United States, 76134