At a glance
ClinicalIndex Comparison RecordN/ACompleted· 157 enrolled
Drug / intervention
Narafilcon B 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.
Assessment of Daily Disposable Silicone Hydrogel Lens Wear
In Brief
A clinical study evaluating Narafilcon B Contact Lens and Spectacles for Myopia. Completed, enrolled 157 participants across 1 site.
Detailed Summary
The purpose of this study is to evaluate the effect of an investigational silicone hydrogel soft contact lens on new contact lens wearers (neophytes) compared to a control of spectacle wearers.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited States
CollaboratorsOhio State University
Timeline
N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartJan 2010
First PostedMar 2010
Primary CompletionApr 2011
TodayJul 2026
First PostedMar 26, 2010
Enrollment StartJan 1, 2010
Primary CompletionApr 1, 2011
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 16.3 years ago
Interventions
Narafilcon B Contact Lensdevice
Spectaclesdevice
spectacle wearers