At a glance
ClinicalIndex Comparison RecordN/ACompleted· 66 enrolled
Drug / intervention
Lehfilcon A contact lenses +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.
Clinical Assessment of a Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lens
In Brief
A clinical study evaluating Lehfilcon A contact lenses, Comfilcon A contact lenses, and 1 other intervention for Myopia. Completed, enrolled 66 participants across 5 sites.
Detailed Summary
The purpose of this study is to assess the clinical performance of an investigational contact lens over 30 days of daily wear.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
202120222023202420252026
First PostedJul 2020
Enrollment StartAug 2020
Primary CompletionNov 2020
TodayJul 2026
First PostedJul 20, 2020
Enrollment StartAug 17, 2020
Primary CompletionNov 18, 2020
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 6.0 years ago
Interventions
Lehfilcon A contact lensesdevice
Investigational silicone hydrogel contact lenses
Comfilcon A contact lensesdevice
Commercially available silicone hydrogel contact lenses
CLEAR CAREdevice
Hydrogen peroxide-based cleaning and disinfecting solution