At a glance
ClinicalIndex Comparison RecordN/ACompleted· 95 enrolled
Drug / intervention
1-DAY ACUVUE® MOIST +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.
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Manufacturing Technology
In Brief
A clinical study evaluating 1-DAY ACUVUE® MOIST for Visual Acuity. Completed, enrolled 95 participants across 6 sites.
Detailed Summary
This study is a multi-site, randomized, double-masked, 2×2 crossover design, 1-week dispensing study. Subjects will wear both Test and Control lenses in each eye in a random order for 1-week each as a daily disposable modality with a wash-out period of 1 week between the wearing periods.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsVisual Acuity
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2020202120222023202420252026
Enrollment StartMay 2019
First PostedMay 2019
Primary CompletionJul 2019
TodayJul 2026
First PostedMay 24, 2019
Enrollment StartMay 15, 2019
Primary CompletionJul 10, 2019
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 7.1 years ago
Interventions
1-DAY ACUVUE® MOISTdevice
etafilcon A contact lenses made with a new manufacturing technology
1-DAY ACUVUE® MOISTdevice
etafilcon A contact lenses made with the current manufacturing technology