Trials / Completed
CompletedNCT01010555
In-vivo Wettability Grading and Assessment Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 25 (actual)
- Sponsor
- CIBA VISION · Industry
- Sex
- All
- Age
- 17 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to investigate the front surface wettability of soft contact lenses while on eye.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | lotrafilcon B | Commercially marketed, silicone hydrogel, spherical contact lens |
| DEVICE | balafilcon A | Commercially marketed, silicone hydrogel, spherical contact lens |
| DEVICE | senofilcon A | Commercially marketed, silicone hydrogel, spherical contact lens |
| DEVICE | enfilcon A | Commercially marketed, silicone hydrogel, spherical contact lens |
Timeline
- Start date
- 2009-10-01
- Primary completion
- 2010-04-01
- Completion
- 2010-04-01
- First posted
- 2009-11-10
- Last updated
- 2012-07-10
- Results posted
- 2011-05-30
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT01010555. Inclusion in this directory is not an endorsement.