Trials / Completed
CompletedNCT01252121
Residence Time Evaluation of Systane Ultra Lubricant Eye Drops vs. Hialid and Saline
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 27 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the ocular retention time of Systane Ultra compared to Hialid and saline.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Systane Ultra Lubricant Eye Drops | One drop in study eye, one time, during office visit. |
| OTHER | Hialid 0.1 Artificial Tears Eye Drops | One drop in study eye, one time, during office visit. |
| OTHER | Unisol 4 Saline Solution | One drop in study eye, one time, during office visit. |
Timeline
- Start date
- 2010-10-01
- Primary completion
- 2011-06-01
- Completion
- 2011-06-01
- First posted
- 2010-12-02
- Last updated
- 2012-10-30
Source: ClinicalTrials.gov record NCT01252121. Inclusion in this directory is not an endorsement.