At a glance
ClinicalIndex Comparison RecordN/ACompleted· 66 enrolled
Drug / intervention
Test 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 Feasibility of a New Silicone Hydrogel Contact Lens
In Brief
A clinical study evaluating Test lens and Air Optix Aqua for Myopia. Completed, enrolled 66 participants across 1 site.
Detailed Summary
The objective of this study is to determine the clinical feasibility and to evaluate the product performance of investigational contact lenses developed by Bausch + Lomb.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
Enrollment StartDec 2010
Primary CompletionDec 2010
Study CompletionJan 2011
First PostedMar 2011
TodayJul 2026
First PostedMar 7, 2011
Enrollment StartDec 1, 2010
Primary CompletionDec 1, 2010
Study CompletionJan 1, 2011
TodayJul 2, 2026
Enrollment to primary: 0 daysPosted 15.3 years ago
Interventions
Test lensdevice
Investigational silicone hydrogel contact lens worn on a daily wear basis
Air Optix Aquadevice
Air Optix Aqua contact lens worn on a daily wear basis