At a glance
ClinicalIndex Comparison RecordN/ACompleted· 126 enrolled
Drug / intervention
Investigational 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 Feasibility of a High Add Multi Focal Contact Lens
In Brief
A clinical study evaluating Investigational contact lens and PureVision 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 the investigational multifocal high add soft contact lens compared with PureVision Multi-focal contact lens on a daily wear basis.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPresbyopia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
Enrollment StartJan 2012
First PostedJan 2012
Primary CompletionFeb 2012
TodayJul 2026
First PostedJan 26, 2012
Enrollment StartJan 1, 2012
Primary CompletionFeb 1, 2012
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 14.4 years ago
Interventions
Investigational contact lensdevice
Worn on a daily wear basis for one week.
PureVision contact lensdevice
Worn on a daily wear basis for one week