Trials / Completed
CompletedNCT03679741
Initial Evaluation of Investigational Lenses Manufactured on a New Production Line
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 126 (actual)
- Sponsor
- Johnson & Johnson Vision Care, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 49 Years
- Healthy volunteers
- Accepted
Summary
This study is a randomized, 4-visit, subject-masked, 2x3 bilateral crossover, dispensing trial. Each study lens will be worn bilaterally in a daily wear (DW) modality for at least 6 hours per day and 5 days per week for approximately two weeks each. The subject will wear either the Test or Control lens twice and the other study lens once.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | CONTROL Lens | Acuvue OASYS |
| DEVICE | TEST Lens | senofilcon A |
Timeline
- Start date
- 2018-08-29
- Primary completion
- 2018-10-31
- Completion
- 2018-10-31
- First posted
- 2018-09-20
- Last updated
- 2019-12-26
- Results posted
- 2019-12-26
Locations
6 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03679741. Inclusion in this directory is not an endorsement.