Trials / Completed
CompletedNCT04631796
Clinical Characterization of an Investigational Soft Silicone Hydrogel Contact Lens
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 36 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The primary objective of this study is to evaluate the overall clinical performance of an investigational silicone hydrogel contact lens over 2 weeks of daily wear.
Detailed description
Participants will attend a Screening visit, a Dispense visit (0 to 4 days later), and a follow-up visit approximately 2 weeks after the Dispense visit.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Lehfilcon A contact lenses | Silicone hydrogel contact lenses with investigational coating |
| DEVICE | Multipurpose disinfection solution | Solution for cleaning, disinfecting, and reconditioning silicone hydrogel contact lenses |
Timeline
- Start date
- 2020-12-03
- Primary completion
- 2020-12-31
- Completion
- 2020-12-31
- First posted
- 2020-11-17
- Last updated
- 2022-01-12
- Results posted
- 2022-01-12
Locations
3 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04631796. Inclusion in this directory is not an endorsement.