At a glance
ClinicalIndex Comparison RecordN/ACompleted· 302 enrolled
Drug / intervention
Investigational Toric Lens +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.
A Study to Evaluate the Performance of Two Designs of Soft Toric Lenses
In Brief
A clinical study evaluating Investigational Toric Lens and PureVision Toric Lens for Myopia. Completed, enrolled 302 participants across 1 site.
Detailed Summary
The objective of the study is to evaluate the product performance of the Bausch + Lomb toric investigational contact lenses compared to the currently marketed PureVision toric contact lenses.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
Enrollment StartDec 2010
Primary CompletionFeb 2011
First PostedMar 2011
Study CompletionApr 2011
TodayJul 2026
First PostedMar 7, 2011
Enrollment StartDec 1, 2010
Primary CompletionFeb 1, 2011
Study CompletionApr 1, 2011
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 15.3 years ago
Interventions
Investigational Toric Lensdevice
Bausch \& Lomb investigational toric contact lens worn on a daily wear basis for 2 weeks.
PureVision Toric Lensdevice
Currently marked Bausch \& Lomb PureVision Toric Lens worn on a daily wear basis for 2 weeks.