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Clinical Performance Comparison of Two Contact Lenses

NCT00975585 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 379

Last updated 2018-06-19

Study results available
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Summary

The purpose of this study is to compare the clinical performance of two contact lenses.

Conditions

  • Myopia

Interventions

DEVICE

senofilcon A

soft contact lens, 2-week replacement indicated

DEVICE

lotrafilcon B

soft contact lens with a 4-week replacement indicated.

Sponsors & Collaborators

  • Visioncare Research Ltd.

    collaborator OTHER

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Principal Investigators

  • Sheila, B Hickson-Curran, BSc, MCOptom · Johnson & Johnson Vision Care, Inc.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2009-08-01
Primary Completion
2009-10-01
Completion
2009-10-01

Countries

  • United States

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 NCT00975585 on ClinicalTrials.gov