NCT01254747

Clinical Evaluation of an Investigational Soft Contact Lens

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 130 (actual)
• Sponsor: CIBA VISION · Industry
• Sex: All
• Age: —
• Healthy volunteers: Not accepted

Summary

The purpose of this 4-week dispensing trial is to evaluate and compare an investigational soft contact lens worn on a daily disposable basis with three other soft contact lenses also worn on a daily disposable basis.

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	Delefilcon A contact lens	Investigational silicone hydrogel, single vision contact lens for daily wear, daily disposable use
DEVICE	Lotrafilcon B contact lens (O2 OPTIX, AIR OPTIX)	Commercially marketed silicone hydrogel, single vision contact lens for daily wear, daily disposable use
DEVICE	Nelfilcon A contact lens (DAILIES AquaComfort Plus)	Commercially marketed hydrogel, single vision contact lens for daily wear, daily disposable use
DEVICE	Narafilcon A contact lens (1-DAY ACUVUE TRUEYE)	Commercially marketed (Europe) silicone hydrogel, single vision contact lens for daily wear, daily disposable use

Timeline

• Start date: 2010-11-01
• Primary completion: 2010-12-01
• Completion: 2010-12-01
• First posted: 2010-12-07
• Last updated: 2012-07-10
• Results posted: 2012-05-17

Locations

2 sites across 2 countries: United States, Germany