Trials / Completed
CompletedNCT07104773
Clinical Investigation of Proclear® 1 Day and MyDay® Sphere Contact Lenses
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 44 (actual)
- Sponsor
- CooperVision International Limited (CVIL) · 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 soft lens wearers.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Control Lens (omafilcon A) | 15 minutes of daily wear |
| DEVICE | Test Lens (stenfilcon A) | 15 minutes of daily wear |
Timeline
- Start date
- 2025-07-24
- Primary completion
- 2025-08-21
- Completion
- 2025-08-21
- First posted
- 2025-08-05
- Last updated
- 2026-04-08
Locations
1 site across 1 country: Canada
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT07104773. Inclusion in this directory is not an endorsement.