Effect of Open Eye Rain® on the tear film and ocular symptoms
Not Applicable
- Conditions
- Observation of the tear film (in healthy volunteers)
- Registration Number
- DRKS00007624
- Lead Sponsor
- Optima Pharmazeutische GmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
healthy subjects
Exclusion Criteria
Contact lens wearer (except lenses removed prior to study) younger than 18years; subjects with ocular defects, degeneration, inflammation; being pregnant, use of artificial tears or ocular medication at day of observation
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ipid layer interference pattern: Observed by tearscope (Keeler) before application and after application at 10min, 30min, 60min, 90min
- Secondary Outcome Measures
Name Time Method tear film stability. Observed by tearscope (Keeler) before application and after application at 10min, 30min, 60min, 90min