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Performance Evaluation of Different Daily Disposable Silicone Hydrogel Contact Lenses

NCT05805059 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 68

Last updated 2024-09-26

Study results available
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Summary

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

Conditions

  • Myopia

Interventions

DEVICE

Control Contact Lens (stenfilcon A)

one week wear

DEVICE

Test Contact Lens (senofilcon A)

one week of wear

Sponsors & Collaborators

  • Centre for Ocular Research & Education, Canada

    collaborator OTHER

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Andrew Sacco · Sacco Eye Group, PLLC

  • Carolyn MacNeil · Insight Eye Care

  • Katherine Bickle · ProCare Vision Center

  • Roxanne Achong-Coan · Coan Eye Care

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
2023-04-14
Primary Completion
2023-06-20
Completion
2023-06-20
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 NCT05805059 on ClinicalTrials.gov