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A Comparative Study of Two Daily Disposable Contact Lenses in Higher Myopia Subjects

NCT02066922 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 19

Last updated 2015-06-08

Study results available
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Summary

The purpose of this study is to compare the change from baseline in central corneal curvature at one week, between 2 silicone hydrogel lenses, in higher myopic subjects.

Conditions

  • Refractive Error
  • Myopia

Interventions

DEVICE

Delefilcon A contact lens

Commercially available silicone hydrogel contact lens

DEVICE

Narafilcon A contact lens

Commercially available silicone hydrogel contact lens

DEVICE

Spectacles

Incremental prescription worn over contact lenses if needed to provide acceptable vision

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Joachim Nick, Dipl. Ing. · Alcon Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-03-31
Primary Completion
2014-05-31
Completion
2014-05-31

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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 NCT02066922 on ClinicalTrials.gov