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Non-dispensing Fitting Study Comparing the Clinical Performance Hydrogel Sphere Design Contact Lenses.

NCT02727816 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 35

Last updated 2018-02-06

Study results available
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Summary

The aim of this non-dispensing study is to evaluate the clinical performance of different hydrogel contact lens designs.

Conditions

  • Myopia

Interventions

DEVICE

filcon IV I (BC 8.6)

control lens

DEVICE

filcon IV I (BC 8.7)

control lens

DEVICE

ocufilcon D

test lens

DEVICE

methafilcon A (BC 8.6)

control lens

DEVICE

methafilcon A (BC 8.7)

control lens

DEVICE

somofilcon A

test lens

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2016-04-30
Primary Completion
2016-05-31
Completion
2016-08-31

Countries

  • Mexico

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 NCT02727816 on ClinicalTrials.gov