Trials / Completed
CompletedNCT02676258
Clinical Comparison of Two Daily Disposable Silicone Hydrogel Soft Contact Lens
A Prospective Randomized Controlled Study to Evaluate the Clinical Performance of Si-Hy Silicone Hydrogel Soft Contact Lens
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Visco Vision Inc. · Industry
- Sex
- All
- Age
- 20 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to evaluate a new daily disposable silicone hydrogel soft contact lens by comparing to an existing daily disposable soft contact lens.
Detailed description
This study is designed to evaluate the performance of the olifilcon B contact lens to demonstrate substantial equivalence to the narafilcon A for regulatory requirement.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Si-Hy (olifilcon B) | Wear Si-Hy silicone hydrgel soft contact lens for 3 months |
| DEVICE | Vistakon (narafilcon A) | Wear Vistakon soft contact lens for 3 months |
Timeline
- Start date
- 2015-06-01
- Primary completion
- 2015-11-01
- Completion
- 2015-11-01
- First posted
- 2016-02-08
- Last updated
- 2016-07-07
Locations
1 site across 1 country: Taiwan
Source: ClinicalTrials.gov record NCT02676258. Inclusion in this directory is not an endorsement.