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A Bilateral Dispensing Comparison of Comfilcon A Over Senofilcon C Contact Lenses

NCT03684928 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2020-06-26

Study results available
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Summary

The aim of this study is to evaluate the subjective acceptance of Comfilcon A contact lenses when worn on a daily wear modality over one month.

Conditions

  • Astigmatism Bilateral

Interventions

DEVICE

Comfilcon A (test)

Daily wear contact lenses

DEVICE

Senofilcon C (control)

Daily wear contact lenses

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Lyndon Jones, PhD FCOptom · Director, Centre for Ocular Research and Education

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-07-23
Primary Completion
2018-12-14
Completion
2019-02-01
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 NCT03684928 on ClinicalTrials.gov