Trials / Terminated
TerminatedNCT01386008
Evaluation of DW Silicone Hydrogel Lens Compared to DW Silicone Hydrogel Lens
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 28 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the performance of the investigational CooperVision silicone hydrogel lens compared to a currently-marketed silicone hydrogel contact lens up to 30 days of daily lens wear.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | senfilcon A contact lens | senofilcon A spherical contact lens worn in a daily wear modality |
| DEVICE | investigational enfilcon A | investigational enfilcon A, worn daily wear modality |
Timeline
- Start date
- 2011-05-01
- Primary completion
- 2011-06-01
- Completion
- 2011-06-01
- First posted
- 2011-06-30
- Last updated
- 2019-09-04
- Results posted
- 2014-03-21
Locations
2 sites across 2 countries: United States, United Kingdom
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT01386008. Inclusion in this directory is not an endorsement.