Comparison of Frequency of Use of Optive and Systane
Phase 4
Completed
- Conditions
- Dry Eye
- Registration Number
- NCT00406510
- Lead Sponsor
- Innovative Medical
- Brief Summary
The purpose of this study is subjectively compare duration of action between Optive and Systane.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- Males or females > 18 years old
- Mild to moderate dry eye symptoms
- Score of at least 2 and no more than 4 on the SESOD at the initial screening visit
- Likely to complete all study visits and able to provide informed consent
Exclusion Criteria
- Current use of topical cyclosporine
- Known contraindications to any study medication or ingredients
- Active ocular diseases or uncontrolled systemic disease (blepharitis patients that are actively being treated or disease that is uncontrollable)
- Ocular surgery within the past 3 months,
- Active ocular allergies
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Private Practice
🇺🇸Azusa, California, United States