DD T2 Daily Disposable Registration Trial
Status: | Completed |
---|---|
Conditions: | Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/24/2019 |
Start Date: | October 12, 2017 |
End Date: | February 21, 2018 |
The purpose of this study is to evaluate the performance of the investigational verofilcon A
contact lens compared to the commercially available delefilcon A contact lens, by assessing
visual acuity as the primary variable.
contact lens compared to the commercially available delefilcon A contact lens, by assessing
visual acuity as the primary variable.
Enrolled participants will be randomized (2:1) to receive either verofilcon A (test) contact
lenses or delefilcon A (control) contact lenses for wear in both eyes and attend 7 office
visits: Baseline, Dispense, 1-week follow-up, 2-week follow-up, 1-month follow-up, 2-month
follow-up and 3-month follow-up/Exit.
lenses or delefilcon A (control) contact lenses for wear in both eyes and attend 7 office
visits: Baseline, Dispense, 1-week follow-up, 2-week follow-up, 1-month follow-up, 2-month
follow-up and 3-month follow-up/Exit.
Inclusion Criteria:
- Successful wear of spherical soft contact lenses for distance correction in both eyes
during the past 3 months for a minimum of 5 days per week and 8 hours per day.
- Best corrected VA 20/25 or better in each eye.
- Other protocol-specified inclusion criteria may apply.
Exclusion Criteria
- Any current or prior wear experience with DT1 lenses.
- Wearing habitual contact lenses in an extended wear modality (routinely sleeping in
lenses for at least 1 night per week) over the last 3 months prior to enrollment.
- Other protocol-specified exclusion criteria may apply.
We found this trial at
6
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