Acute Comfort and Blur of Systane Ultra and Systane
Not Applicable
Completed
- Conditions
- Dry Eye
- Registration Number
- NCT00748865
- Lead Sponsor
- Alcon Research
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
- Documented diagnosis of dry eye
Exclusion Criteria
- Use of contact lens within 7 days preceding enrollment
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Primary Outcome Measures
Name Time Method Drop Comfort once upon instillation Drop comfort grading scale is a 0 to 9 scale, with 0 meaning most comfortable and 9 meaning most uncomfortable,
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie the efficacy of Systane Ultra in dry eye syndrome compared to Systane?
How does Systane Ultra's formulation improve corneal hydration versus standard artificial tears like Systane?
What biomarkers correlate with patient preference for Systane Ultra in dry eye clinical trials?
Are there specific adverse event profiles for Systane Ultra versus Systane in dry eye treatment?
How do Systane Ultra and Systane compare to other PEG-based artificial tears in dry eye management?
Trial Locations
- Locations (1)
Contact Alcon Call Center for Trial Location
🇺🇸Fort Worth, Texas, United States
Contact Alcon Call Center for Trial Location🇺🇸Fort Worth, Texas, United States