Status:

COMPLETED

Evaluation of Daily Disposable Lenses With Multi-Purpose Solution (MPS)

Lead Sponsor:

Alcon Research

Conditions:

Myopia

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The purpose of this study is to 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.

Detailed Description

Corneal staining and subjective responses for ocular redness and comfort will be compared.

Eligibility Criteria

Inclusion

  • 18 years of age or older.
  • Visual acuity correctable to 20/30 (Snellen) or better in each eye at distance with contact lenses.
  • Successfully wearing hydrogel or silicone hydrogel contact lenses on a daily wear basis for at least two weeks prior to study.
  • Other protocol-defined inclusion criteria may apply.

Exclusion

  • History of hypersensitivity to any components of the multi-purpose solution.
  • Evidence or history of ocular conditions as prescribed in protocol.
  • One functional eye or a monofit lens
  • Any slit-lamp finding score equal to 1 at Visit 1 of each study period.
  • Significant corneal staining at visit 1 of each study period as prescribed in protocol.
  • Other protocol-defined exclusion criteria may apply.

Key Trial Info

Start Date :

January 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 1 2008

Estimated Enrollment :

64 Patients enrolled

Trial Details

Trial ID

NCT00733291

Start Date

January 1 2008

End Date

February 1 2008

Last Update

December 28 2011

Active Locations (1)

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Contact Alcon Call Center for Trial Locations

Fort Worth, Texas, United States, 76134