NCT04096898

Senofilcon A Lenses in Moderate to Severe Dry Eye Disease

Clinical Trial to Determine Whether Senofilcon A Lenses Provide Relief of Symptoms and Signs in Patients With Moderate to Severe Dry Eye Disease

• Status: Unknown
• Phase: N/A
• Study type: Interventional
• Enrollment: 32 (estimated)
• Sponsor: University of Illinois at Chicago · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

A clinical trial using Senofilcon A daily lenses in the treatment of moderate to severe dry eye. This a comparison between signs and symptoms prior to and during treatment.

Detailed description

32 patients with moderate to severe dry eye will be enrolled in this short-term proof of concept study to determine the efficacy in using soft lenses made of Senofilcon A in reducing signs and symptoms.

Conditions

• Moderate to Severe Dry Eye Disease

Interventions

Type	Name	Description
DEVICE	Senofilcon A contact lens	Senofilcon lenses will be tested in moderate to severe dry eye patients to determine their efficacy in reducing discomfort associated with dry eye.

Timeline

• Start date: 2018-04-23
• Primary completion: 2020-12-31
• Completion: 2020-12-31
• First posted: 2019-09-20
• Last updated: 2020-03-24

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study