Trials / Completed
CompletedNCT01449526
A Study to Evaluate the Safety and Efficacy of a New Silicone Hydrogel Contact Lens Design
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 166 (actual)
- Sponsor
- Bausch & Lomb Incorporated · Industry
- Sex
- All
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to evaluate the safety and efficacy of a new silicone hydrogel contact lens compared to the Bausch + Lomb PureVision contact lens when worn by adapted soft contact lens wearers.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | B&L Investigational Contact Lens | Lenses will be worn on a daily wear basis for 3 months, new lenses dispensed monthly. |
| DEVICE | B&L PureVision Contact Lens | Lenses will be worn on a daily wear basis for 3 months, new lenses dispensed monthly. |
Timeline
- Start date
- 2011-08-01
- Primary completion
- 2011-12-01
- Completion
- 2012-01-01
- First posted
- 2011-10-10
- Last updated
- 2015-02-18
- Results posted
- 2015-02-18
Source: ClinicalTrials.gov record NCT01449526. Inclusion in this directory is not an endorsement.