NCT03305770

DD T2 Daily Disposable Registration Trial

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 107 (actual)
• Sponsor: Alcon Research · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

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.

Detailed description

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.

Conditions

• Myopia
• Refractive Errors

Interventions

Type	Name	Description
DEVICE	verofilcon A contact lenses	Daily disposable soft contact lenses
DEVICE	delefilcon A contact lenses	Daily disposable soft contact lenses

Timeline

• Start date: 2017-10-12
• Primary completion: 2018-02-21
• Completion: 2018-02-21
• First posted: 2017-10-10
• Last updated: 2019-02-22
• Results posted: 2019-02-22

Locations

6 sites across 1 country: United States

Regulatory

• FDA-regulated device study