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

NCT05166902 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 67

Last updated 2023-07-27

Study results available
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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.

Conditions

  • Ametropia

Interventions

DEVICE

Lens A (comfilcon A lens)

1 month

DEVICE

Lens B (lehfilcon A lens)

1 month

Sponsors & Collaborators

  • Centre for Ocular Research & Education, Canada

    collaborator OTHER

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • David Wilkinson · Spadina Optometry

  • Roxanne Achong-Coan · Coan Eyecare

  • Fiona Soong · Eyes on Sheppard Clinic

  • Mike Cymbor · Nittany 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
Yes

Timeline & Regulatory

Start
2022-01-31
Primary Completion
2022-07-09
Completion
2022-07-09
FDA Device
Yes

Countries

  • United States
  • Canada

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 NCT05166902 on ClinicalTrials.gov