Trials / Completed
CompletedNCT00829751
The Physiological Consequence of Silicone-hydrogel Care-solution Bio-incompatibility
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 26 (actual)
- Sponsor
- Southern California College of Optometry at Marshall B. Ketchum University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to more objectively evaluate potential lens-material/care solution bio-incompatibilities. We will do this by measuring corneal staining and the amount of fluorescein dye diffusion into the eye.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | PureVision lenses soaked in ReNu Multiplus | Purevision silicone hydrogel lenses |
| DEVICE | PureVision lenses soaked in OptiFree RePlenish | Purevision silicone hydrogel lenses soaked in OptiFree RePlenish |
Timeline
- Start date
- 2008-11-01
- Primary completion
- 2011-06-01
- Completion
- 2011-06-01
- First posted
- 2009-01-27
- Last updated
- 2013-06-04
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00829751. Inclusion in this directory is not an endorsement.