N/A
N=20
Acute Comfort and Blurring Profile Evaluation of Marketed Lubricant Eye Drops
Dry Eye
Bottom Line
View on ClinicalTrials.gov: NCT00756093 ↗Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Mar 2010
Primary outcome: Primary: Drop Comfort — 0.7; 1.05; 1.84; 1.1 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Systane Ultra Lubricant Eye Drops (Other); Optive Lubricant Eye Drops (Other); Blink Tears (Other); GenTeal Moderate Lubricant Eye Drops (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Alcon Research
- Primary completion
- Sep 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Drop Comfort |
0.7; 1.05; 1.84; 1.1 | — |
Summary
To evaluate drop comfort, acceptability and blur profile between four marketed artificial tears in dry eye patients
Eligibility Criteria
Inclusion Criteria
- documented diagnosis of dry eye
Exclusion Criteria
- use of topical ocular drops within 2 hours preceding enrollment
Data sourced from ClinicalTrials.gov (NCT00756093). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.