Trials / Completed
CompletedNCT02696317
Clinical Evaluation of ACUVUE® OASYS® 1-Day and ACUVUE® OASYS®
Clinical Evaluation of ACUVUE® OASYS® 1-Day Daily Disposable Silicone Hydrogel Contact Lenses
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 84 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the performance of two commercially-available silicone hydrogel contact lenses in normal and low humidity environments after at least 7 days of wear.
Detailed description
After randomization to lens order, subjects attended study visits that included a 3 hour exposure to reduced humidity environment (20% relative humidity) and subsequent tear film assessments for each study lens.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Senofilcon A contact lenses with HydraLuxe™ | Contact lenses worn during Period 1 or 2, as randomized |
| DEVICE | Senofilcon A contact lenses | Contact lenses worn during Period 1 or 2, as randomized |
Timeline
- Start date
- 2016-03-18
- Primary completion
- 2016-06-06
- Completion
- 2016-06-06
- First posted
- 2016-03-02
- Last updated
- 2018-07-02
- Results posted
- 2017-06-26
Source: ClinicalTrials.gov record NCT02696317. Inclusion in this directory is not an endorsement.