At a glance
ClinicalIndex Comparison RecordN/ACompleted· 126 enrolled
Drug / intervention
LD118033 contact 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 Product Performance of a Low Add MultiFocal Soft Contact Lens
In Brief
A clinical study evaluating LD118033 contact lens and PureVision multifocal contact lens for Presbyopia. Completed, enrolled 126 participants across 1 site.
Detailed Summary
The objective of this study is to evaluate the product performance of an investigational multifocal low add soft contact lens.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPresbyopia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
Enrollment StartJan 2012
Primary CompletionFeb 2012
First PostedFeb 2012
Study CompletionMar 2012
TodayJul 2026
First PostedFeb 27, 2012
Enrollment StartJan 1, 2012
Primary CompletionFeb 1, 2012
Study CompletionMar 1, 2012
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 14.3 years ago
Interventions
LD118033 contact lensdevice
Multifocal contact lens worn on a daily wear basis for 1 week
PureVision multifocal contact lensdevice
PureVision multifocal contact lens worn on a daily wear basis for 1 week.