A Clinical Study Comparing the Comfort of Three Commercially Available Contact Lenses

NCT02298400 · clinicaltrials.gov ↗

NA

Phase

WITHDRAWN

Status

INDUSTRY

Sponsor class

Stopped Study terminated by Sponsor

Conditions

Contact Lens Complication

Interventions

DEVICE: Acuvue® Oasys® Lenses (senofilcon A)
DEVICE: 30-Day Bausch + Lomb PureVision (balafilcon A)
DEVICE: Clariti® 1-Day (Somofilcon A)

Sponsor

ORA, Inc.