At a glance
ClinicalIndex Comparison RecordN/ACompleted· 67 enrolled
Drug / intervention
Lens A (comfilcon A 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.
Evaluation of Monthly Replacement Lens Designs in Habitual Soft Contact Lens Wearers Who Report Frequent Digital Devise Use
In Brief
A clinical study evaluating Lens A (comfilcon A lens) and Lens B (lehfilcon A lens) for Ametropia. Completed, enrolled 67 participants across 4 sites in 2 countries.
Detailed Summary
To evaluate the clinical performance of two monthly silicone hydrogel contact lenses in habitual wearers of frequent replacement (FRP) lenses when worn for 1-month.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAmetropia
CountriesCanada, United States
CollaboratorsCentre for Ocular Research & Education, Canada
Timeline
N/ACompletedFinished
20222023202420252026
First PostedDec 2021
Enrollment StartJan 2022
Primary CompletionJul 2022
TodayJul 2026
First PostedDec 22, 2021
Enrollment StartJan 31, 2022
Primary CompletionJul 9, 2022
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 4.5 years ago
Interventions
Lens A (comfilcon A lens)device
1 month
Lens B (lehfilcon A lens)device
1 month