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Clinical Evaluation of an Investigational Soft Contact Lens

NCT01254747 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 130

Last updated 2012-07-10

Study results available
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Summary

The purpose of this 4-week dispensing trial is to evaluate and compare an investigational soft contact lens worn on a daily disposable basis with three other soft contact lenses also worn on a daily disposable basis.

Conditions

  • Myopia

Interventions

DEVICE

Delefilcon A contact lens

Investigational silicone hydrogel, single vision contact lens for daily wear, daily disposable use

DEVICE

Lotrafilcon B contact lens (O2 OPTIX, AIR OPTIX)

Commercially marketed silicone hydrogel, single vision contact lens for daily wear, daily disposable use

DEVICE

Nelfilcon A contact lens (DAILIES AquaComfort Plus)

Commercially marketed hydrogel, single vision contact lens for daily wear, daily disposable use

DEVICE

Narafilcon A contact lens (1-DAY ACUVUE TRUEYE)

Commercially marketed (Europe) silicone hydrogel, single vision contact lens for daily wear, daily disposable use

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-11-30
Primary Completion
2010-12-31
Completion
2010-12-31

Countries

  • United States
  • Germany

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 NCT01254747 on ClinicalTrials.gov