Trials / Withdrawn
WithdrawnNCT02298400
A Clinical Study Comparing the Comfort of Three Commercially Available Contact Lenses
A Single-Center, Cross-over, Pilot Study Evaluating Acuvue® Oasys® Lenses (Senofilcon A), 30-Day Bausch + Lomb PureVision (Balafilcon A), and Clariti® 1-Day (Somofilcon A) Lenses, for Their Impact on Ocular Discomfort Induced by Exposure to the Turbo Controlled Adverse Environment™
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- ORA, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the comfort of three commercially available contact lenses.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Acuvue® Oasys® Lenses (senofilcon A) | Contact lenses placed in each eye during the day for about 8 hours |
| DEVICE | 30-Day Bausch + Lomb PureVision (balafilcon A) | Contact lenses placed in each eye during the day for about 8 hours |
| DEVICE | Clariti® 1-Day (Somofilcon A) | Contact lenses placed in each eye during the day for about 8 hours |
Timeline
- Start date
- 2014-08-01
- Primary completion
- 2014-09-01
- Completion
- 2014-09-01
- First posted
- 2014-11-24
- Last updated
- 2024-04-25
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02298400. Inclusion in this directory is not an endorsement.