CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 63 enrolled
Drug / intervention
PureVision2 HD contact lenses +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/NCT01416142
NCT01416142N/ACompleted

A Study to Evaluate the Product Performance of the PureVision®2 HD Contact Lens

Bausch & Lomb Incorporated·interventional·Posted Aug 12, 2011·Updated Dec 25, 2013

In Brief

A clinical study evaluating PureVision2 HD contact lenses and Spectacles for Myopia. Completed, enrolled 63 participants across 1 site.

Detailed Summary

The objective of this study is to evaluate the product performance of PureVision2 HD contact lenses.

Study Details

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

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedAug 12, 2011
Enrollment StartJul 1, 2011
Primary CompletionAug 1, 2011
Study CompletionSep 1, 2011
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 14.9 years ago

Interventions

PureVision2 HD contact lensesdevice

Lenses to be worn through 1/2 of an HD movie. Following the movie, all subjects were to wear the dispensed contact lenses on a daily wear basis for approximately one week.

Spectaclesdevice

Spectacles to be worn throughout 1/2 of an HD movie.