NCT02637804

Daily Disposable Silicone Hydrogel Contact Lens, Stenfilcon A, Clinical Study

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 106 (actual)
• Sponsor: CooperVision, Inc. · Industry
• Sex: All
• Age: 18 Years – 40 Years
• Healthy volunteers: Not accepted

Summary

Clinical evaluation of stenfilcon A compared with narafilcon A and delefilcon A This is a total 120 subject, randomized, open label, bilateral wear, two week crossover study (each lens for 1 week) evaluating the clinical performance of stenfilcon A spherical lenses compared to narafilcon A or delefilcon A spherical lenses.

Detailed description

The aim of this study is to evaluate the clinical performance of stenfilcon A compared with narafilcon A and delefilcon A. The study participants will be allocated to two parallel groups (Group 1 and Group 2), 60 subjects each, based on the control lenses, narafilcon A and delefilcon A spherical lenses. Study groups: Group 1: stenfilcon A vs. narafilcon A Group 2: stenfilcon A vs. delefilcon A

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	stenfilcon A	contact lens
DEVICE	narafilcon A	contact lens
DEVICE	delefilcon A	contact lens

Timeline

• Start date: 2016-01-01
• Primary completion: 2016-03-01
• Completion: 2016-08-01
• First posted: 2015-12-22
• Last updated: 2017-10-23
• Results posted: 2017-10-23