Trials / Completed
CompletedNCT02771145
Clinical Evaluation of the Safety and Efficacy of FID 120947A
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 91 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 20 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the safety and efficacy of FID 120947A in soft contact lens wearers of Japanese ethnicity.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | FID 120947A contact lens disinfecting solution | Investigational 3% hydrogen peroxide solution that uses a platinum catalyst for neutralization and is intended for simultaneous cleaning, protein removal, disinfecting and storage of silicone hydrogel and soft contact lenses |
| DEVICE | Soft contact lenses (SCL) | Commercially available soft contact lenses worn a minimum of 8 hours each day on a daily wear basis for the duration of the study (180 days). A fresh pair will be dispensed on Day 0, Day 30, Day 60, and Day 135. |
| DEVICE | SCL preservative solution | Commercially available solution for rinsing soft contact lenses |
Timeline
- Start date
- 2016-05-20
- Primary completion
- 2017-01-10
- Completion
- 2017-01-10
- First posted
- 2016-05-12
- Last updated
- 2019-01-10
- Results posted
- 2018-10-15
Locations
1 site across 1 country: Japan
Source: ClinicalTrials.gov record NCT02771145. Inclusion in this directory is not an endorsement.