Trials / Completed

CompletedNCT05166902

Evaluation of Monthly Replacement Lenses in Habitual Soft Contact Lens Wearers Who Report Frequent Digital Devise Use

Evaluation of Monthly Replacement Lens Designs in Habitual Soft Contact Lens Wearers Who Report Frequent Digital Devise Use

Status: Completed
Phase: N/A
Study type: Interventional
Enrollment: 67 (actual)

Sponsor: CooperVision, Inc. · Industry
Sex: All
Age: 18 Years – 35 Years
Healthy volunteers: Accepted

Summary

To evaluate the clinical performance of two monthly silicone hydrogel contact lenses in habitual wearers of frequent replacement (FRP) lenses when worn for 1-month.

Detailed description

This study is a prospective, bilateral eye, double-masked, randomized, 1-month cross-over, daily-wear design involving two different FRP lens types. Each lens type will be worn for approximately one month.

Conditions

Ametropia

Interventions

Type	Name	Description
DEVICE	Lens A (comfilcon A lens)	1 month
DEVICE	Lens B (lehfilcon A lens)	1 month

Timeline

Start date: 2022-01-31
Primary completion: 2022-07-09
Completion: 2022-07-09
First posted: 2021-12-22
Last updated: 2023-07-27
Results posted: 2023-07-27

Locations

4 sites across 2 countries: United States, Canada

Regulatory

FDA-regulated device study

Source: ClinicalTrials.gov record NCT05166902. Inclusion in this directory is not an endorsement.