Trials / Completed
CompletedNCT06817785
Soft Lens Study: Biomedics 1 Day Extra Sphere and Clariti 1 Day Sphere
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 45 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this study is to evaluate and compare the performance of two soft contact lenses.
Detailed description
The aim of this study is to evaluate and compare the performance of a hydrogel lens and a silicone hydrogel lens in existing myopic soft lens wearers.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Lens 1 (ocufilcon D) | 15 minutes of daily wear |
| DEVICE | Lens 2 (somofilcon A) | 15 minutes of daily wear |
Timeline
- Start date
- 2025-01-24
- Primary completion
- 2025-02-25
- Completion
- 2025-02-25
- First posted
- 2025-02-10
- Last updated
- 2026-04-08
Locations
1 site across 1 country: Canada
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06817785. Inclusion in this directory is not an endorsement.