Clinical Evaluation of MyDay™ and 1-DAY ACUVUE® TruEye®
| Status: | Completed |
|---|---|
| Conditions: | Ocular |
| Therapuetic Areas: | Ophthalmology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/13/2015 |
| Start Date: | April 2015 |
| End Date: | August 2015 |
| Contact: | Alcon Call Center |
| Email: | alcon.medinfo@alcon.com |
| Phone: | 1-888-451-3937 |
Clinical Evaluation of MyDay™ Daily Disposable Silicone Hydrogel Contact Lenses
The purpose of this study is to evaluate the functional vision of 2 daily disposable
silicone hydrogel contact lenses using Time Controlled Visual Acuity (TCVA) measurements at
high luminance and high contrast after 10+/-3 days of wear post 3 hour exposure to a reduced
humidity environment.
silicone hydrogel contact lenses using Time Controlled Visual Acuity (TCVA) measurements at
high luminance and high contrast after 10+/-3 days of wear post 3 hour exposure to a reduced
humidity environment.
After randomization, participants will attend a baseline visit to include a 3 hour exposure
to reduced humidity environment.
to reduced humidity environment.
Inclusion Criteria:
- Must sign informed consent form.
- Adapted, current soft silicone hydrogel daily disposable contact lens wearer during
the last 2 months.
- Willing to wear lenses every day or at least 5 days per week 6 hours per day.
- Willing to discontinue artificial tears and rewetting drops usage on the days of
study visits.
- Other protocol-specified inclusion criteria may apply.
Exclusion Criteria:
- Monocular (only 1 eye with functional vision) or fit with only 1 lens.
- Pregnant or lactating.
- Current MyDay™ or 1DAY ACUVUE® TruEye® lens wearer.
- Any abnormal ocular condition as specified in the protocol.
- Other protocol-specified exclusion criteria may apply.
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