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

Not Applicable
Completed
Conditions
Dry Eye
Registration Number
NCT01139372
Lead Sponsor
Alcon Research
Brief Summary

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

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
96
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
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)Day 7
Secondary Outcome Measures
NameTimeMethod

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