Acute Comfort and Blur Profile of a Lubricant Eye Drop Versus a Marketed Eye Ointment
Primary Purpose
Dry Eye
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Lubricant eye drop FID 115958D
Refresh PM Ointment
Sponsored by
About this trial
This is an interventional treatment trial for Dry Eye focused on measuring Dry eye, artificial tears
Eligibility Criteria
Inclusion Criteria:
- Documented diagnosis of dry eye
Exclusion Criteria:
- Must not have worn contact lenses within 12 hours preceding enrollment
- Must not have used any topical ocular drops or ointment within 24 hours preceding enrollment
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Lubricant eye drop
Refresh PM Ointment
Arm Description
Lubricant eye drop
Refresh PM Ointment
Outcomes
Primary Outcome Measures
Three-minute visual blur profile
Overall Acceptability
Secondary Outcome Measures
Drop Comfort Upon Instillation
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01076998
Brief Title
Acute Comfort and Blur Profile of a Lubricant Eye Drop Versus a Marketed Eye Ointment
Study Type
Interventional
2. Study Status
Record Verification Date
January 2012
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
January 2010 (Actual)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Alcon Research
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to compare the comfort and blurriness of the investigational lubricant eye drop with a marketed artificial tear ointment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dry Eye
Keywords
Dry eye, artificial tears
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
24 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Lubricant eye drop
Arm Type
Experimental
Arm Description
Lubricant eye drop
Arm Title
Refresh PM Ointment
Arm Type
Active Comparator
Arm Description
Refresh PM Ointment
Intervention Type
Other
Intervention Name(s)
Lubricant eye drop FID 115958D
Intervention Description
1 drop in each eye, one time
Intervention Type
Other
Intervention Name(s)
Refresh PM Ointment
Intervention Description
1 drop in each eye, one time
Primary Outcome Measure Information:
Title
Three-minute visual blur profile
Time Frame
Through 3 minutes (post-instillation)
Title
Overall Acceptability
Time Frame
Immediately upon instillation
Secondary Outcome Measure Information:
Title
Drop Comfort Upon Instillation
Time Frame
Immediately upon installation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Documented diagnosis of dry eye
Exclusion Criteria:
Must not have worn contact lenses within 12 hours preceding enrollment
Must not have used any topical ocular drops or ointment within 24 hours preceding enrollment
12. IPD Sharing Statement
Learn more about this trial
Acute Comfort and Blur Profile of a Lubricant Eye Drop Versus a Marketed Eye Ointment
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