Trials / Completed
CompletedNCT05779072
Dual Focus Soft Contact Lens Wear Cessation Study
MiSight Lens Wear Cessation Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 83 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 14 Years – 19 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to investigate the effect of ceasing treatment with dual focus soft contact lenses.
Detailed description
This is a bilateral, open label, dispensing study with subjects who have completed dual focus soft contact lens wear treatment for either 3 or 6 years and who are refit to Proclear 1-day lens for 1 year.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Single Vision Soft Contact Lens | Subjects refit to Single Vision Soft Contact Lens for 1 year |
Timeline
- Start date
- 2019-03-01
- Primary completion
- 2021-03-01
- Completion
- 2021-03-01
- First posted
- 2023-03-22
- Last updated
- 2023-11-01
- Results posted
- 2023-11-01
Locations
4 sites across 4 countries: Canada, Portugal, Singapore, United Kingdom
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05779072. Inclusion in this directory is not an endorsement.