At a glance
ClinicalIndex Comparison RecordN/ACompleted· 144 enrolled
Drug / intervention
Investigational Lens +2 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 Investigational Lens, Acuvue Oasys Lens, and 1 other intervention for Myopia. Completed, enrolled 144 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 lens.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
Enrollment StartNov 2010
Primary CompletionDec 2010
Study CompletionJan 2011
First PostedMar 2011
TodayJul 2026
First PostedMar 4, 2011
Enrollment StartNov 1, 2010
Primary CompletionDec 1, 2010
Study CompletionJan 1, 2011
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 15.3 years ago
Interventions
Investigational Lensdevice
Bausch \& Lomb investigational silicone hydrogel lens on a daily wear basis for 1 week.
Acuvue Oasys Lensdevice
Johnson \& Johnson Acuvue Oasys contact lens on a daily wear basis for 1 week.
Air Optix Aqua Lensdevice
Ciba Vision Air Optix Aqua contact lens on a daily wear basis for 1 week.