Trials / Completed
CompletedNCT00597467
Study of Soft Contact Lens Use With 7 Day Extended Wear
An Open-Labeled, Multi-Center, Randomized Investigation of the VISA (Comfilcon A) Silicone Hydrogel Soft (Hydrophilic) Contact Lens for Use in a 7 Day Extended Wear Regimen
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 460 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
To compare the safety and efficacy of the CVI silicone-hydrogel lens worn on an extended wear basis for a period of up to 7 days and 6 nights with the Acuvue 2 soft contact lenses.
Detailed description
To compare the safety and efficacy of the CVI silicone-hydrogel lens worn on an extended wear basis for a period of up to 7 days and 6 nights with the Acuvue 2 soft contact lenses in this open-labeled randomized study.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | VISA (comfilcon A) Silicone Hydrogel Soft contact lens | Test device |
| DEVICE | Acuvue 2 Soft Contact Lens | Control device |
Timeline
- Start date
- 2006-03-01
- Primary completion
- 2007-11-01
- Completion
- 2007-11-01
- First posted
- 2008-01-18
- Last updated
- 2020-07-17
Locations
23 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT00597467. Inclusion in this directory is not an endorsement.