Evaluation of an Investigational Multifocal Lens

NCT02223754 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 371

Last updated 2018-06-19

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to test the performance of an investigational multifocal test soft contact lens.

Conditions

Interventions

DEVICE

lotrafilcon B

Soft contact lens to be worn as daily wear, monthly replacement modality.

DEVICE

etafilcon A

Soft contact lens to be worn as daily wear, daily disposable modality.

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2014-08-31
Primary Completion
2014-11-30
Completion
2014-11-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT02223754 on ClinicalTrials.gov