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Study of ACUVUE® ADVANCE® PLUS Contact Lenses.

NCT01244893 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 44

Last updated 2018-06-19

Study results available
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Summary

The purpose of this study is to compare ACUVUE® ADVANCE® Plus contact lenses made prior to process qualification (prePQ) against the ACUVUE® ADVANCE® Plus lenses made after the process qualification (postPQ).

Conditions

  • Myopia

Interventions

DEVICE

Acuvue Advance Plus prePQ

silicone hydrogel contact lens manufactured prior to equipment process qualification activities.

DEVICE

Acuvue Advance Plus postPQ

silicone hydrogel contact lens manufactured after equipment process qualification activities.

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2010-10-31
Primary Completion
2010-11-30

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 NCT01244893 on ClinicalTrials.gov