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Non-dispensing Study to Check Prescription Equivalence of Two Daily Disposable Toric Contact Lens Types

NCT01120782 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2018-06-19

Study results available
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Summary

The purpose of this study is to determine whether the prescription determined for a new daily disposable toric contact lens will be a good match to a prescription determined for an existing brand of lens.

Conditions

  • Astigmatism

Interventions

DEVICE

etafilcon A toric contact lens with new wetting agent

Investigational toric contact lens made of etafilcon A material with a new wetting agent.

DEVICE

etafilcon A toric contact lens

Marketed toric contact lens made of etafilcon A material.

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2010-02-01
Primary Completion
2010-02-01
Completion
2010-02-01
FDA Device
Yes

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 NCT01120782 on ClinicalTrials.gov