Trials / Completed
CompletedNCT03635528
Evaluating Accommodative Responses of Soft Contact Lenses for Myopia Control
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 11 (actual)
- Sponsor
- Johnson & Johnson Vision Care, Inc. · Industry
- Sex
- All
- Age
- 7 Years – 25 Years
- Healthy volunteers
- Accepted
Summary
This is a bilateral, non-dispensing, randomized, controlled, double-masked, 7x7 cross-over study. Each subject will be bilaterally fitted with one of the 7 test articles in each of the 7 periods for a total of four visits. Up to two lens types will be fit at each of the four study visits.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Test Lens 1 | EMO-114 |
| DEVICE | Test Lens 2 | EMO-116 |
| DEVICE | Test Lens 3 | EMO-118 |
| DEVICE | Test Lens 4 | RMY-100 |
| DEVICE | Test Lens 5 | Biofinity multifocal D Lens |
| DEVICE | Control Lens 1 | EMO-117 |
| DEVICE | Control Lens 2 | Proclear 1 day |
Timeline
- Start date
- 2018-11-29
- Primary completion
- 2019-07-18
- Completion
- 2019-07-18
- First posted
- 2018-08-17
- Last updated
- 2020-08-20
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03635528. Inclusion in this directory is not an endorsement.