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Evaluation of Vision Effects of a Cosmetic Tinted Hydrogel Contact Lens

NCT02886923 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2019-12-20

Study results available
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Summary

Subjects will wear 2 of 2 study contact lenses for a wearing time of approximately three to four hours at each of the visits in order to take measurements on binocular functional visual performance.

Conditions

  • Refractive Error

Interventions

DEVICE

Hioxifilcon A Test

contact lens made with hioxifilcon A material

DEVICE

Hioxifilcon A With Cosmetic Ring Control

contact lens made with hioxifilcon A material with a cosmetic ring on the lens

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
35 Years
Max Age
42 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-08-01
Primary Completion
2017-01-23
Completion
2017-01-23
FDA Device
Yes

Countries

  • United Kingdom

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 NCT02886923 on ClinicalTrials.gov