NCT02251561

Clinical Evaluation of Opti-Free III (FID 109182) Compared to Opti-Free Plus® in Japan

Clinical Evaluation of Opti-Free III Compared to Opti-Free Plus®

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 36 (actual)
• Sponsor: Alcon Research · Industry
• Sex: All
• Age: 20 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to compare an investigational contact lens care product (FID 109182) to a commercially available contact lens product (Opti-Free Plus®) for corneal staining when used with Acuvue® Oasys® contact lenses. The contact lenses will be pre-soaked in the products for 24-48 hours prior to a 2-hour contralateral wear period.

Conditions

• Corneal Staining

Interventions

Type	Name	Description
DEVICE	FID 109182	Investigational multipurpose contact lens cleaning and disinfecting solution
DEVICE	Opti-Free Plus	Commercially available multipurpose contact lens cleaning and disinfecting solution
DEVICE	Senofilcon A contact lens	Commercially available silicone hydrogel contact lens

Timeline

• Start date: 2013-11-01
• Primary completion: 2014-05-01
• Completion: 2014-05-01
• First posted: 2014-09-29
• Last updated: 2015-06-10
• Results posted: 2015-06-10