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Clinical Comparison of Two Silicone-Hydrogel Contact Lenses

NCT00762385 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 97

Last updated 2018-06-19

Study results available
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Summary

The objective of this study is to evaluate the clinical performance of two silicone-hydrogel contact lenses.

Conditions

  • Refractive Error

Interventions

DEVICE

galyfilcon A

galyfilcon A

DEVICE

comfilcon A

comfilcon A

Sponsors & Collaborators

  • Foresight Regulatory Strategies, Inc.

    collaborator INDUSTRY

  • Visioncare Research Ltd.

    collaborator OTHER

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
39 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-08-31
Primary Completion
2007-10-31
Completion
2007-10-31

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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 NCT00762385 on ClinicalTrials.gov