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Non-Dispensing Evaluation of an Investigational Galyfilcon A Soft Contact Lens

NCT01054807 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2018-06-19

No results posted yet for this study

Summary

The purpose of this investigation is to compare the fit characteristics and vision attributes of an investigational Galyfilcon A contact lens and an approved Galyfilcon A contact lens.

Conditions

  • Myopia

Interventions

DEVICE

Galyfilcon A Habitual Lens

Comparison of three soft contact lens designs.

DEVICE

Galyfilcon A 8.7 BC (Investigational)

Comparison of three soft contact lens designs.

DEVICE

Galyfilcon A 8.3 BC (Investigational)

Comparison of three soft contact lens designs

Sponsors & Collaborators

  • Coles-Brennan Pty Ltd

    collaborator UNKNOWN

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Principal Investigators

  • Noel Brennan, McOptom PhD · Coles-Brennan Pty Ltd

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-11-01
Primary Completion
2010-03-01
Completion
2010-03-01
FDA Device
Yes

Countries

  • Australia

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 NCT01054807 on ClinicalTrials.gov