N/A
N=20
Acute Comfort and Blur of Systane Ultra and Systane
Dry Eye
Bottom Line
View on ClinicalTrials.gov: NCT00748865 ↗Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Mar 2010
Primary outcome: Primary: Drop Comfort — 0.55; 0.60 Units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Systane Ultra Lubricant Eye Drops (Other); Systane Lubricant Eye Drops (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Alcon Research
- Primary completion
- Aug 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Drop Comfort |
0.55; 0.60 | — |
Summary
To evaluate drop comfort, acceptability, preference and blue profile between two marketed artificial tears in both dry eyes and non-dry eye patient population.
Eligibility Criteria
Inclusion Criteria
- Documented diagnosis of dry eye
Exclusion Criteria
- Use of contact lens within 7 days preceding enrollment
Data sourced from ClinicalTrials.gov (NCT00748865). 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.