NCT03351101

Clinical Study of Approved Contact Lenses

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 271 (actual)
• Sponsor: Bausch & Lomb Incorporated · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Accepted

Summary

Evaluation of Johnson \& Johnson Acuvue Vita (senofilcon C) soft contact lenses to the Bausch + Lomb Ultra (samfilcon A) soft contact lenses

Detailed description

to compare the performance of currently marketed Johnson \& Johnson Acuvue Vita (senofilcon C) soft contact lenses to the currently marketed Bausch + Lomb Ultra (samfilcon A) soft contact lenses among adapted wearers of Acuvue Oasys soft contact lenses.

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	Senofilcon C	Senofilcon C Contact Lens
DEVICE	Samfilcon A	Samfilcon A Contact Lens

Timeline

• Start date: 2017-10-23
• Primary completion: 2017-11-10
• Completion: 2017-12-08
• First posted: 2017-11-22
• Last updated: 2021-01-08
• Results posted: 2020-09-16

Locations

11 sites across 1 country: United States

Regulatory

• FDA-regulated device study