Trials / Completed
CompletedNCT04901897
Product Performance of a New Silicone Hydrogel Contact Lens
A Study to Evaluate the Product Performance of a New Silicone Hydrogel Contact Lens
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 805 (actual)
- Sponsor
- Bausch & Lomb Incorporated · Industry
- Sex
- All
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to evaluate the product performance of kalifilcon A, compared to the Johnson \& Johnson Acuvue Oasys® 1-Day with HydraLuxe™ (senofilcon A) daily disposable contact lens and Alcon DAILIES TOTAL1® (delefilcon A) daily disposable contact lenses when worn by current soft contact lens wearers on a daily disposable wear basis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | kalifilcon A | kalifilcon A daily disposable contact lens |
| DEVICE | delefilcon A | DAILIES TOTAL1® (delefilcon A) daily disposable contact lenses |
| DEVICE | senofilcon A | Acuvue Oasys® 1-Day with HydraLuxe™ (senofilcon A) daily disposable contact lens |
Timeline
- Start date
- 2019-07-31
- Primary completion
- 2019-10-09
- Completion
- 2019-10-09
- First posted
- 2021-05-26
- Last updated
- 2021-07-08
- Results posted
- 2021-07-08
Locations
35 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04901897. Inclusion in this directory is not an endorsement.