MedTrace Logo

A Comparison of Two Daily Disposable Soft Contact Lenses

NCT02427477 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2018-06-19

Study results available
· View outcomes & findings →

Summary

Approximately 120 subjects will be comparing two soft contact lenses for one week each.

Conditions

  • Visual Acuity

Interventions

DEVICE

senofilcon A

Subjects will wear the contact lenses in both eyes for seven days

DEVICE

delefilcon A

Subjects will wear the contact lenses in both eyes for seven days

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2015-04-30
Completion
2015-04-30

Countries

  • United States

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 NCT02427477 on ClinicalTrials.gov