Trials / Completed
CompletedNCT00946777
Barrier Function Measurement in Dry Eye Patients After Using Systane Ultra for 30 Days
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 19 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The primary objective is to determine if there is a correlation between reductions in corneal staining and improvements in corneal barrier function.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Systane® Ultra | Systane® Ultra 1-2 drops, 4 times per day for 30 days |
Timeline
- Start date
- 2009-07-01
- Primary completion
- 2009-09-01
- Completion
- 2009-09-01
- First posted
- 2009-07-27
- Last updated
- 2016-11-18
Source: ClinicalTrials.gov record NCT00946777. Inclusion in this directory is not an endorsement.