MedTrace Logo

Daily Disposable Performance of 1•DAY ACUVUE® TruEye™ and 1•DAY ACUVUE® MOIST® With LACREON® TECHNOLOGY

NCT01467557 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1171

Last updated 2018-06-19

Study results available
· View outcomes & findings →

Summary

This study is an observational registry of patients who have recently been prescribed 1•DAY ACUVUE® TruEye® or 1•DAY ACUVUE® MOIST® Brand Contact Lenses with LACREON® TECHNOLOGY.

Conditions

  • Myopia
  • Hyperopia

Interventions

DEVICE

narafilcon B daily disposable soft contact lenses

daily disposable soft contact lenses

DEVICE

etafilcon A daily disposable soft contact lenses

daily disposable soft contact lenses

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Eligibility

Min Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-10-31
Primary Completion
2013-10-31
Completion
2013-10-31

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 NCT01467557 on ClinicalTrials.gov