Trials / Completed
CompletedNCT05431478
Clinical Performance of Two Reusable Silicone Hydrogel Contact Lenses
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 68 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to assess the clinical performance of two reusable silicone hydrogel contact lenses when worn on a daily wear basis.
Detailed description
In this crossover study, subjects will wear each study lens type for approximately 14 days and attend 7 scheduled visits. The expected duration of subject participation in the study is approximately 28 days (approximately 14 days per each study lens type).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Serafilcon A contact lenses | Reusable silicone hydrogel contact lenses worn during the day and removed at night for daily cleaning and disinfection |
| DEVICE | Senofilcon A contact lenses | Reusable silicone hydrogel contact lenses worn during the day and removed at night for daily cleaning and disinfection |
| DEVICE | CLEAR CARE | Hydrogen peroxide based contact lens cleaning and disinfecting solution |
Timeline
- Start date
- 2022-07-15
- Primary completion
- 2022-09-09
- Completion
- 2022-09-09
- First posted
- 2022-06-24
- Last updated
- 2023-09-21
- Results posted
- 2023-09-21
Locations
5 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05431478. Inclusion in this directory is not an endorsement.