MedTrace Logo

Performance Comparison of Two Monthly Replacement Silicone Hydrogel Multifocal Lens Types

NCT06232590 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-02-12

Study results available
· View outcomes & findings →

Summary

To evaluate and compare the performance of two monthly replacement multifocal contact lenses in existing wearers.

Conditions

Interventions

DEVICE

Control Lens (comfilcon A)

Multifocal monthly replacement contact lens for 1 month

DEVICE

Test Lens (lehfilcon A)

Multifocal monthly replacement contact lens for 1 month

Sponsors & Collaborators

  • Centre for Ocular Research & Education, Canada

    collaborator OTHER

  • CooperVision International Limited (CVIL)

    lead INDUSTRY

Principal Investigators

  • Andrew Sacco · Sacco Eye Group

  • David Wilkinson · Spadina Optometry

  • Katherine Bickle · ProCare Vision Center

  • Dustin Gardner · New Bremen EyeCare

  • Gina Wesley · Complete Eye Care of Medina

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
42 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-23
Primary Completion
2024-07-09
Completion
2024-07-09
FDA Device
Yes

Countries

  • United States
  • Canada

Study Locations

More Related Trials

Entities

Diseases

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 NCT06232590 on ClinicalTrials.gov