Trials / Completed
CompletedNCT04050618
Evaluation Of One Silicone Hydrogel Contact Lens and Two Hydrogel Lenses in Daily Wear
Multi-Center Cross-Over Evaluation Of Avaira Vitality Silicone Hydrogel Contact Lens and Two Hydrogel Lenses in Daily Wear
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 114 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
To evaluate the comparative clinical performance of the fanfilcon A silicone hydrogel lens used in daily wear and to compare this with competitive hydrogel lens products.
Detailed description
This 8-week, subject-masked, bilateral, two-part, cross-over evaluation will compare the clinical performance of fanfilcon A silicone hydrogel contact lens and competitive hydrogel contact lenses when worn daily. Lenses will be replaced either on a 2-weekly or 4-weekly basis, depending on control lens group.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | fanfilcon A test lens | Silicone hydrogel contact lens |
| DEVICE | ocufilcon D control lens | hydrogel contact lens |
| DEVICE | etafilcon A control lens | hydrogel contact lens |
Timeline
- Start date
- 2019-06-09
- Primary completion
- 2019-09-24
- Completion
- 2019-11-08
- First posted
- 2019-08-08
- Last updated
- 2020-10-19
- Results posted
- 2020-10-19
Locations
6 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04050618. Inclusion in this directory is not an endorsement.