An Evaluation of the Daytime Use of an Investigational Lubricant Eye Drop
Not Applicable
Completed
- Conditions
- Dry Eye
- Interventions
- Other: FID 115958D (Lubricant Eye Drop)
- 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
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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
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description FID 115958D FID 115958D (Lubricant Eye Drop) Lubricant eye drop
- Primary Outcome Measures
Name Time Method 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
Name Time Method