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Performance Evaluation of Daily Disposable Contact Lenses in Habitual Lens Wearers Who Use Digital Devices Frequently

NCT05805150 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 69

Last updated 2024-06-25

Study results available
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Summary

The goal of this study is to compare the performance of two daily disposable silicone hydrogel lenses.

Conditions

  • Myopia

Interventions

DEVICE

Control Lens (stenfilcon A)

One week wear

DEVICE

Test Lens (senofilcon A)

One week wear

Sponsors & Collaborators

  • Centre for Ocular Research & Education, Canada

    collaborator OTHER

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Gina Wesley · Complete Eye Care of Medina

  • Michael Cymbor · Nittany Eye Associates

  • Shane Kannarr · Kannarr Eye Care

  • Stephen Montaquila · West Bay Eye Associates

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-13
Primary Completion
2023-06-01
Completion
2023-06-01
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05805150 on ClinicalTrials.gov