Trials / Completed
CompletedNCT00934102
Ophthalmic Compatibility During Seven Days of Continuous Wear of Silicone Hydrogel Lenses
Ophthalmic Compatibility During Seven Days of Continuous Wear of Silicone Hydrogel Lenses (P/318/08/C)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 57 (actual)
- Sponsor
- CIBA VISION · Industry
- Sex
- All
- Age
- 17 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to assess the ophthalmic compatibility of three different silicone hydrogel lenses worn on an overnight basis for six nights.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Narafilcon A contact lens | Investigational, silicone hydrogel, spherical soft contact lens |
| DEVICE | Lotrafilcon A contact lens | Commercially marketed, silicone hydrogel, spherical soft contact lens |
| DEVICE | Galyfilcon A contact lens | Commercially marketed, silicone hydrogel, spherical soft contact lens |
Timeline
- Start date
- 2009-08-01
- Primary completion
- 2009-09-01
- Completion
- 2009-09-01
- First posted
- 2009-07-08
- Last updated
- 2012-07-10
- Results posted
- 2010-12-01
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT00934102. Inclusion in this directory is not an endorsement.