Trials / Completed
CompletedNCT02394808
2-week Evaluation of Marketed Silicone Hydrogel Contact Lenses in Indian Population
2-week Dispensing Cross-Over Evaluation of Marketed Silicone Hydrogel Contact Lenses in an Indian Population
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 54 (actual)
- Sponsor
- Johnson & Johnson Vision Care, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 39 Years
- Healthy volunteers
- Accepted
Summary
The primary objective of this study is to evaluate the clinical performance of two marketed silicone hydrogel contact lenses in an Indian population in the following areas: physiological characteristics, comfort characteristics and vision characteristics.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | senofilcon A | One fresh pair of contact lenses worn for 11 (+/-2) days, for a minimum of 6 hours per day |
| DEVICE | lotrafilcon B | One fresh pair of contact lenses worn for 11 (+/-2) days, for a minimum of 6 hours per day |
Timeline
- Start date
- 2015-01-01
- Primary completion
- 2015-09-01
- Completion
- 2015-09-01
- First posted
- 2015-03-20
- Last updated
- 2018-06-19
- Results posted
- 2017-06-19
Locations
1 site across 1 country: India
Source: ClinicalTrials.gov record NCT02394808. Inclusion in this directory is not an endorsement.