Trials / Completed
CompletedNCT04201639
Evaluating the Performance of Precision1 Daily Disposable Contact Lens in a Group of Heavy Digital Device Users
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- University of Waterloo · Academic / Other
- Sex
- All
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the performance of Precision1 DD CLs with regard to subjective symptoms (dryness, comfort, vision), lens fit and time to haze in CL wearers who identify themselves as heavy digital devices users (at least 6 hours of digital device use per day).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Verofilcon A contact lenses | Daily disposable silicone hydrogel contact lenses indicated for the optical correction of refractive ametropia (myopia and hyperopia) |
Timeline
- Start date
- 2019-12-13
- Primary completion
- 2021-09-27
- Completion
- 2021-09-27
- First posted
- 2019-12-17
- Last updated
- 2023-01-26
- Results posted
- 2023-01-26
Locations
1 site across 1 country: Canada
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04201639. Inclusion in this directory is not an endorsement.