At a glance
ClinicalIndex Comparison RecordN/ACompleted· 36 enrolled
Drug / intervention
Lehfilcon A 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.
Pilot Clinical Performance of a Silicone Hydrogel Lens for Up to Six Nights of Extended Wear
In Brief
A clinical study evaluating Lehfilcon A contact lens and Comfilcon A contact lens for Refractive Errors and 2 related conditions. Completed, enrolled 36 participants across 3 sites.
Detailed Summary
The purpose of this clinical study is to evaluate the on-eye performance of an investigational soft contact lens compared to a commercially available soft contact lens when worn continuously for up to 1 week.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRefractive Errors, Myopia, Hyperopia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
202120222023202420252026
First PostedMay 2020
Enrollment StartAug 2020
Primary CompletionAug 2020
TodayJul 2026
First PostedMay 27, 2020
Enrollment StartAug 3, 2020
Primary CompletionAug 31, 2020
TodayJul 2, 2026
Enrollment to primary: 28 daysPosted 6.1 years ago
Interventions
Lehfilcon A contact lensdevice
Investigational silicone hydrogel contact lens
Comfilcon A contact lensdevice
Commercially available silicone hydrogel contact lens