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Open Eye Corneal Swelling With Daily Disposable Contact Lenses and no Lens Wear

NCT01765972 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 39

Last updated 2018-06-19

Study results available
· View outcomes & findings →

Summary

The primary purpose of this clinical trial is to evaluate the eye's response to three test soft contact lenses as well as no lens wear, with respect to Corneal Staining.

Conditions

  • Corneal Swelling

Interventions

DEVICE

etafilcon A with Lacreon

contact lens with Lacreon

DEVICE

etafilcon A with Lacreon with print

contact lens with Lacreon and cosmetic print

DEVICE

etafilcon A with print

contact lens with print

DEVICE

Spectacles (habitual)

Spectacles

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-12-31
Primary Completion
2013-05-31
Completion
2013-05-31

Countries

  • Canada

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 NCT01765972 on ClinicalTrials.gov