NCT01695369

Evaluation of Comfilcon A and Senofilcon A Lenses

Clinical Comfort Evaluation of Biofinity and Acuvue Oasys Lenses

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 61 (actual)
• Sponsor: CooperVision, Inc. · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

Evaluation of Comfilcon A and Senofilcon A Lenses

Detailed description

Non-dispensing, single-masked, randomized, contralateral study comparing the test lens against the control lens. Each subject will be randomized to wear the test lens in one eye and the control lens in the other eye.

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	Senofilcon A; Comfilcon A	Senofilcon A; Comfilcon A
DEVICE	Comfilcon A; Senofilcon A	Comfilcon A; Senofilcon A

Timeline

• Start date: 2012-08-01
• Primary completion: 2012-08-01
• Completion: 2012-08-01
• First posted: 2012-09-28
• Last updated: 2020-07-28
• Results posted: 2014-03-06

Locations

1 site across 1 country: United States