NCT02568254

Evaluation of Three Daily Disposable Contact Lenses

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 78 (actual)
• Sponsor: Johnson & Johnson Vision Care, Inc. · Industry
• Sex: All
• Age: 18 Years – 40 Years
• Healthy volunteers: Accepted

Summary

This is a single-site, 8-visit, double-masked, cross-over study involving three marketed products as study lenses. Participants will be randomly assigned each lens type, which will be worn for approximately two weeks (12 +/- 2 days) each. Participants will undergo a minimum washout period of 3 days before entering the study and undergo a minimum 7 day washout period between dispensing each lens type.

Conditions

• Visual Acuity

Interventions

Type	Name	Description
DEVICE	Lens 1 (etafilcon A)	Each lens type will be worn for approximately 2 weeks (12 +/- 2 days).
DEVICE	Lens 2 (nelfilcon A)	Each lens type will be worn for approximately 2 weeks (12 +/- 2 days).
DEVICE	Lens 3 (nesofilcon A)	Each lens type will be worn for approximately 2 weeks (12 +/- 2 days).

Timeline

• Start date: 2015-09-03
• Primary completion: 2016-01-18
• Completion: 2016-01-18
• First posted: 2015-10-05
• Last updated: 2017-07-17
• Results posted: 2017-07-17

Locations

1 site across 1 country: Canada

Regulatory

• FDA-regulated device study