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Clinical Evaluation of Proclear Toric and Biofinity Toric

NCT06431061 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 37

Last updated 2025-09-15

Study results available
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Summary

The aim of this study is to compare the short-term clinical performance of two Toric contact lenses.

Conditions

  • Astigmatism

Interventions

DEVICE

Lens A (omafilcon B)

15 minutes of daily wear.

DEVICE

Lens B (comfilcon A)

15 minutes of daily wear.

Sponsors & Collaborators

  • Centre for Ocular Research & Education, Canada

    collaborator OTHER

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Lyndon Jones · Centre for Ocular Research and Education

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-04
Primary Completion
2024-11-13
Completion
2024-11-13
FDA Device
Yes

Countries

  • 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 NCT06431061 on ClinicalTrials.gov