NCT00756093CompletedNot Applicable
Acute Comfort and Blurring Profile Evaluation of Marketed Lubricant Eye Drops
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Alcon Research
- Enrollment
- 20
- Locations
- 1
- Primary Endpoint
- Drop Comfort
Study Overview
Brief Summary
To evaluate drop comfort, acceptability and blur profile between four marketed artificial tears in dry eye patients
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Crossover
- Primary Purpose
- Treatment
- Masking
- Double (Participant, Investigator)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •documented diagnosis of dry eye
Exclusion Criteria
- •use of topical ocular drops within 2 hours preceding enrollment
Arms & Interventions
Optive Lubricant Eye Drops
Active Comparator
Optive Lubricant Eye Drops 1 drop each eye one time
Intervention: Optive Lubricant Eye Drops (Other)
GenTeal Moderate Lubricant Eye Drops
Active Comparator
GenTeal Moderate Lubricant Eye Drops 1 drop each eye one time
Intervention: GenTeal Moderate Lubricant Eye Drops (Other)
Blink Tears
Active Comparator
Blink Tears 1 drop each eye one time
Intervention: Blink Tears (Other)
Systane Ultra Lubricant Eye Drops
Experimental
Systane Ultra Lubricant Eye Drops 1 drop each one time
Intervention: Systane Ultra Lubricant Eye Drops (Other)
Outcomes
Primary Outcomes
Drop Comfort
Time Frame: once upon instillation
Drop comfort grading scale is a 0 to 9 scale, with 0 meaning most comfortable and 9 meaning most uncomfortable.
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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