CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 44 enrolled
Drug / intervention
Acuvue Advance Plus prePQ +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01244893
NCT01244893N/ACompleted
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Study of ACUVUE® ADVANCE® PLUS Contact Lenses.

Johnson & Johnson Vision Care, Inc.·interventional·Posted Nov 19, 2010·Updated Jun 19, 2018

In Brief

A clinical study evaluating Acuvue Advance Plus prePQ and Acuvue Advance Plus postPQ for Myopia. Completed, enrolled 44 participants across 3 sites.

Detailed 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).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedNov 19, 2010
Enrollment StartOct 1, 2010
Primary CompletionNov 1, 2010
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 15.6 years ago

Interventions

Acuvue Advance Plus prePQdevice

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

Acuvue Advance Plus postPQdevice

silicone hydrogel contact lens manufactured after equipment process qualification activities.