CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 379 enrolled
Drug / intervention
senofilcon A +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/NCT00975585
NCT00975585N/ACompleted
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Clinical Evaluation of Two Silicone Hydrogel Frequent Replacement Contact Lenses

Johnson & Johnson Vision Care, Inc.·interventional·Posted Sep 11, 2009·Updated Jun 19, 2018

In Brief

A clinical study evaluating senofilcon A and lotrafilcon B for Myopia. Completed, enrolled 379 participants across 25 sites.

Detailed Summary

The purpose of this study is to compare the clinical performance of two contact lenses.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited States
CollaboratorsVisioncare Research Ltd.

Timeline

N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedSep 11, 2009
Enrollment StartAug 1, 2009
Primary CompletionOct 1, 2009
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 16.8 years ago

Interventions

senofilcon Adevice

soft contact lens, 2-week replacement indicated

lotrafilcon Bdevice

soft contact lens with a 4-week replacement indicated.