Trials / Completed
CompletedNCT04050605
Refitting Somofilcon A Toric Contact Lens Wearers Into Fanfilcon A Toric Lenses for 4-weeks of Wear
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this prospective study is to evaluate the clinical performance of habitual wearers of Clariti Toric lenses after a refit with Avaira Vitality Toric lenses for 1-month of daily wear.
Detailed description
The aim of this prospective study is to evaluate the clinical performance of habitual wearers of Clariti Toric lenses after a refit with Avaira Vitality Toric lenses for 1-month of daily wear. This is a prospective, subject masked; bilateral, 1-month refit study comparing the fitting characteristics of Clariti Toric silicone hydrogel lenses, (somofilcon A); against Avaira Vitality silicone hydrogel Toric lenses (fanfilcon A).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | somofilcon A toric contact lens | Contact Lens |
| DEVICE | fanfilcon A toric contact lens | Contact Lens |
Timeline
- Start date
- 2019-06-04
- Primary completion
- 2019-08-16
- Completion
- 2019-10-18
- First posted
- 2019-08-08
- Last updated
- 2020-09-09
- Results posted
- 2020-08-28
Locations
1 site across 1 country: Mexico
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04050605. Inclusion in this directory is not an endorsement.