NCT01951703

Senofilcon A Investigational Manufacturing Process

Clinical Investigation of Senofilcon A Manufactured Using an Alternate Hydration Process

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 136 (actual)
• Sponsor: Johnson & Johnson Vision Care, Inc. · Industry
• Sex: All
• Age: 18 Years – 70 Years
• Healthy volunteers: Not accepted

Summary

To evaluate the impact of a new contact lens hydration process

Detailed description

To evaluate the impact on clinical performance of senofilcon A lenses manufactured using an alternate hydration process and compare the performance with senofilcon A lenses manufactured using the current process.

Conditions

• Visual Acuity
• Comfort
• Overall Vision

Interventions

Type	Name	Description
DEVICE	senofilcon A	Control, senfilcon A
DEVICE	senofilcon A	Test, senofilcon A

Timeline

• Start date: 2013-09-01
• Primary completion: 2013-12-01
• Completion: 2013-12-01
• First posted: 2013-09-27
• Last updated: 2018-06-19
• Results posted: 2015-08-03

Locations

4 sites across 1 country: United States