CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 510 enrolled
Drug / intervention
PureVision Contact Lens +2 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/NCT00640341
NCT00640341Phase 4Completed

Product Performance of Bausch & Lomb PureVision® Contact Lens When Compared to Johnson & Johnson Acuvue Oasys Contact Lens and the Ciba Vision O2Optix Contact Lens Worn Daily.

Bausch & Lomb Incorporated·interventional·Posted Mar 21, 2008·Updated Dec 12, 2011

In Brief

A Phase 4 clinical trial evaluating PureVision Contact Lens, Acuvue Oasys Contact Lens, and 1 other intervention for Myopia. Completed, enrolled 510 participants across 1 site.

Detailed Summary

The objective of this study is to evaluate the performance of the PureVision Contact Lens compared to Acuvue Oasys Contact lens and O2Optix Contact lens when worn on a daily wear basis.

Study Details

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

Timeline

Phase 4CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMar 21, 2008
Enrollment StartFeb 1, 2008
Primary CompletionApr 1, 2008
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 18.3 years ago

Interventions

PureVision Contact Lensdevice

contact lens for daily wear

Acuvue Oasys Contact Lensdevice

contact lens for daily wear

O2Optix Contact lensdevice

contact lens for daily wear