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Investigation of Ocular Signs & Symptoms in Wearers Fitted With Contact Lenses Following Digital Device Use

NCT02394756 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2018-06-19

Study results available
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Summary

The objective of this study is to assess how various silicone hydrogel lenses perform when worn by subjects who are heavy digital device users.

Conditions

  • Visual Performance

Interventions

DEVICE

Marketed Soft Contact lens

Replacement schedule every 2 weeks

DEVICE

AIR OPTIX® AQUA

Replacement schedule every 4 weeks

DEVICE

Biofinity®

Replacement schedule every 4 weeks

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2015-02-28
Primary Completion
2015-09-30
Completion
2015-09-30

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 NCT02394756 on ClinicalTrials.gov