NCT02066922

A Comparative Study of Two Daily Disposable Contact Lenses in Higher Myopia Subjects

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 19 (actual)
• Sponsor: Alcon Research · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to compare the change from baseline in central corneal curvature at one week, between 2 silicone hydrogel lenses, in higher myopic subjects.

Detailed description

Participants were expected to attend 4 office visits. Visit 1 was the Screening/Enrollment visit. At Visit 2 (Baseline Visit), participants were randomized and the study lenses were trial fit. At Visit 3 (Dispense Visit), participants received study lenses for approximately 1 week of wear. Visit 4 was the Exit visit. Expected duration of participation in the study was 3 weeks.

Conditions

• Refractive Error
• Myopia

Interventions

Type	Name	Description
DEVICE	Delefilcon A contact lens	Commercially available silicone hydrogel contact lens
DEVICE	Narafilcon A contact lens	Commercially available silicone hydrogel contact lens
DEVICE	Spectacles	Incremental prescription worn over contact lenses if needed to provide acceptable vision

Timeline

• Start date: 2014-03-01
• Primary completion: 2014-05-01
• Completion: 2014-05-01
• First posted: 2014-02-20
• Last updated: 2015-06-08
• Results posted: 2015-06-08