An Evaluation of the Daytime Use of an Investigational Lubricant Eye Drop

Overview

The purpose of this study is to describe the subjective assessments of an investigational lubricant eye drop.

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Non-Randomized
    • Intervention Model: Single Group Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: June 2010

Interventions

  • Other: FID 115958D (Lubricant Eye Drop)
    • 1 drop in each eye at least twice daily

Arms, Groups and Cohorts

  • Experimental: FID 115958D
    • Lubricant eye drop

Clinical Trial Outcome Measures

Primary Measures

  • Daytime Use Assessment: “I would use this product at bedtime for my dry eye symptoms” Likert scale (i.e. strongly disagree, disagree, neither disagree nor agree, agree, strongly agree)
    • Time Frame: Day 7

Participating in This Clinical Trial

Inclusion Criteria

  • Documented diagnosis of dry eye – Current use of Refresh Liquigel, GenTeal Gel Drops or Refresh Celluvisc at least twice daily Exclusion Criteria:

  • Must not have worn contact lenses within 7 days preceding enrollment – Must not have had punctal plugs inserted within 30 days preceding enrollment

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Alcon Research
  • Provider of Information About this Clinical Study
    • Sponsor

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