At a glance
ClinicalIndex Comparison RecordN/ACompleted· 114 enrolled
Drug / intervention
LID220365 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.
Clinical Performance Assessment of Two Silicone Hydrogel Daily Disposable Contact Lenses
In Brief
A clinical study evaluating LID220365 contact lens and LID006961 contact lens for Refractive Errors and Myopia. Completed, enrolled 114 participants across 7 sites.
Detailed Summary
The purpose of this study is to assess the overall clinical performance of a contact lens made with a modified manufacturing process.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRefractive Errors, Myopia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
202420252026
First PostedFeb 2023
Enrollment StartJun 2023
Primary CompletionJun 2023
TodayJul 2026
First PostedFeb 13, 2023
Enrollment StartJun 2, 2023
Primary CompletionJun 27, 2023
TodayJul 2, 2026
Enrollment to primary: 25 daysPosted 3.4 years ago
Interventions
LID220365 contact lensdevice
Investigational delefilcon A spherical contact lens made with a modified manufacturing process
LID006961 contact lensdevice
Commercially available delefilcon A spherical contact lens