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Clinical Evaluation Of Two Daily Disposable Contact Lenses And A Monthly Replacement Lens

NCT01151371 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 452

Last updated 2018-06-19

Study results available
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Summary

The objective of the study is to compare the clinical performance of silicone hydrogel daily disposable contact lenses, conventional hydrogel daily disposable contact lenses and silicone hydrogel monthly replacement contact lenses.

Conditions

  • Myopia

Interventions

DEVICE

narafilcon B contact lens

Silicone Hydrogel Daily Disposable Contact Lenses

DEVICE

nelfilcon A contact lens

Conventional Hydrogel Daily Disposable Contact Lenses

DEVICE

lotrafilcon B contact lens

Silicone Hydrogel Monthly Replacement Contact Lenses

Sponsors & Collaborators

  • Visioncare Research Ltd.

    collaborator OTHER

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2010-02-01
Primary Completion
2010-04-01
Completion
2010-04-01

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 NCT01151371 on ClinicalTrials.gov