At a glance
ClinicalIndex Comparison RecordN/ACompleted· 22 enrolled
Drug / intervention
LID011121 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 of a Silicone Hydrogel Following Six Nights of Extended Wear
In Brief
A clinical study evaluating LID011121 contact lens and Comfilcon A contact lens for Refractive Errors. Completed, enrolled 22 participants across 2 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 following 1 week of extended wear.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRefractive Errors
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20192020202120222023202420252026
First PostedAug 2018
Enrollment StartAug 2018
Primary CompletionSep 2018
TodayJul 2026
First PostedAug 3, 2018
Enrollment StartAug 23, 2018
Primary CompletionSep 11, 2018
TodayJul 2, 2026
Enrollment to primary: 18 daysPosted 7.9 years ago
Interventions
LID011121 contact lensdevice
Investigational silicone hydrogel contact lens
Comfilcon A contact lensdevice
Commercially available silicone hydrogel contact lens