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Clinical Evaluation of Hydrogels vs Silicone Hydrogel Contact Lenses

NCT01966770 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2020-07-30

Study results available
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Summary

The aim of this fitting study is to evaluate the clinical performance of different hydrogel and silicone hydrogel contact lenses.

Conditions

  • Myopia

Interventions

DEVICE

Pair 1 (ocufilcon D / ocufilcon D)

Randomized to contra lateral lens pair 1 (ocufilcon D hydrogel / ocufilcon D hydrogel)

DEVICE

Pair 2 (ocufilcon D / enfilcon A)

Randomized to contra lateral lens pair 2 (ocufilcon D hydrogel / enfilcon A silicone)

DEVICE

Pair 3 (ocufilcon D / comfilcon A)

Randomized to contra lateral lens pair 3 (ocufilcon D hydrogel / comfilcon A silicone)

DEVICE

Pair 4 (methafilcon A / methafilcon A)

Randomized to contra lateral lens pair 4 (methafilcon A hydrogel sphere / methafilcon A hydrogel asphere)

DEVICE

Pair 5 (methafilcon A / comfilcon A)

Randomized to contra lateral lens pair 5 (methafilcon A hydrogel / comfilcon A silicone)

DEVICE

Pair 6 (omafilcon A / comfilcon A)

Randomized to contra lateral lens pair 6 (omafilcon A hydrogel / comfilcon A silicone)

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Meng Lin, OD PhD FAAO · CRC-UC Berkeley

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-10-31
Primary Completion
2013-11-30
Completion
2013-11-30

Countries

  • United States

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 NCT01966770 on ClinicalTrials.gov