DD T2 Daily Disposable Registration Trial

Completed · Not applicable

Conditions studied: Myopia, Refractive Errors

In brief

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.

Key facts

Study ID

NCT03305770

Run by

Alcon Research

People needed

107

Starts

2017-10-12

Expected to finish

2018-02-21

Last updated by the study team

2019-02-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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.

Where it is running

• Alcon Investigative Site — San Diego, California, United States
• Alcon Investigative Site — Longwood, Florida, United States
• Alcon Investigative Site — Maitland, Florida, United States
• Alcon Investigative Site — Bloomington, Illinois, United States
• Alcon Investigative Site — Brentwood, Tennessee, United States
• Alcon Investigative Site — Memphis, Tennessee, United States

Full record on ClinicalTrials.gov

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