Trials / Completed
CompletedNCT03969290
Clinical Performance of Two Daily Disposable Contact Lenses - Study 1
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 69 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate end of day (EOD) visual acuity (VA) at distance when wearing Precision1™ contact lenses compared to Acuvue® Moist contact lenses.
Detailed description
The expected duration of subject participation in the study is 1-8 days, with 3 scheduled visits (Screening, Dispense, Exit).
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) |
| DEVICE | Etafilcon A contact lenses | Daily disposable contact lenses indicated for the optical correction of refractive ametropia (myopia and hyperopia) |
Timeline
- Start date
- 2019-06-05
- Primary completion
- 2019-08-05
- Completion
- 2019-08-05
- First posted
- 2019-05-31
- Last updated
- 2019-08-22
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT03969290. Inclusion in this directory is not an endorsement.