At a glance
ClinicalIndex Comparison RecordN/ACompleted· 253 enrolled
Drug / intervention
senofilcon A 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.
Design Validation of Senofilcon A With New UV-blocking Additive
In Brief
A clinical study evaluating senofilcon A TEST Lens and senofilcon A CONTROL Lens for Visual Acuity. Completed, enrolled 253 participants across 10 sites.
Detailed Summary
This is a 2-visit, multi-site, partially subject-masked, 2-arm parallel, controlled, randomized and dispensing trial. Subjects will be randomized to one of two study lenses for the entire duration of the study. The study lenses will be worn for a period of 2 weeks each in a bilateral fashion.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsVisual Acuity
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20192020202120222023202420252026
Enrollment StartOct 2018
First PostedOct 2018
Primary CompletionNov 2018
TodayJul 2026
First PostedOct 16, 2018
Enrollment StartOct 1, 2018
Primary CompletionNov 1, 2018
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 7.7 years ago
Interventions
senofilcon A TEST Lensdevice
JJVC Investigational Contact Lens
senofilcon A CONTROL Lensdevice
Acuvue Oasys