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Clinical Validation of the New Print on Focus DAILIES Toric

NCT01097863 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 280

Last updated 2012-07-10

Study results available
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Summary

The purpose of this study is to validate the improvements to the inversion indicator.

Conditions

  • Myopia

Interventions

DEVICE

nelfilcon A contact lens, modified inversion indicator

Investigational, nelfilcon A, toric, soft contact lens for daily disposable wear, with modified inversion indicator

DEVICE

nelfilcon A contact lens, no inversion indicator

Investigational, nelfilcon A, toric, soft contact lens for daily disposable wear, with no inversion indicator

DEVICE

nelfilcon A contact lens, inversion indicator

Commercially marketed, nelfilcon A, toric, soft contact lens for daily disposable wear, with inversion indicator

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2010-05-31
Completion
2010-05-31

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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 NCT01097863 on ClinicalTrials.gov