MedTrace Logo

Clinical Performance Comparison of Several Different Contact Lenses

NCT00912028 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 71

Last updated 2018-06-19

Study results available
· View outcomes & findings →

Summary

The purpose of the study is to evaluate the possible benefits of second generation silicone hydrogel contact lenses.

Conditions

  • Myopia

Interventions

DEVICE

senofilcon A

contact lens

DEVICE

lotrafilcon B

contact lens

DEVICE

balafilcon A

contact lens

DEVICE

methafilcon A

contact lens

DEVICE

vifilcon A

contact lens

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Principal Investigators

  • Carlos E Leite Arieta, MD, PhD · Associate Professor - Ophthalmolgy, University of Campinas, Brazil

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2009-05-01
Primary Completion
2010-02-01
Completion
2010-02-01

Countries

  • Brazil

Study Locations

More Related Trials

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 NCT00912028 on ClinicalTrials.gov