NCT05050578

Clinical Assessment of Two Reusable Silicone Hydrogel Contact Lenses

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 166 (actual)
• Sponsor: Alcon Research · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to compare the clinical performance of LID018869 soft contact with ACUVUE® OASYS with HYDRACLEAR® PLUS (AOHP) soft contact lenses over 30 days of daily wear.

Detailed description

Subjects will be expected to attend 6 visits. Subjects will be expected to wear their study contact lenses every day for at least 10 hours per day over a 30-day period for each study lens type. The total duration of a subject's participation in the study will be approximately 65 days.

Conditions

• Refractive Errors

Interventions

Type	Name	Description
DEVICE	Lehfilcon A contact lenses	Commercially available, silicone hydrogel, spherical contact lenses used as indicated
DEVICE	Senofilcon A contact lenses	Commercially available, silicone hydrogel, spherical contact lenses used as indicated
DEVICE	CLEAR CARE	Hydrogen peroxide-based contact lens cleaning and disinfecting solution

Timeline

• Start date: 2021-11-02
• Primary completion: 2022-02-22
• Completion: 2022-02-22
• First posted: 2021-09-20
• Last updated: 2023-03-16
• Results posted: 2023-03-16

Locations

10 sites across 1 country: United States

Regulatory

• FDA-regulated device study