At a glance
ClinicalIndex Comparison RecordN/ACompleted· 53 enrolled
Drug / intervention
Lens A (fanfilcon A) +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.
Performance Evaluation of Reusable Contact Lenses When Worn For One Month By Habitual Soft Contact Lens Wearers
In Brief
A clinical study evaluating Lens A (fanfilcon A) and Lens B (lotrafilcon B) for Myopia and Hyperopia. Completed, enrolled 53 participants across 3 sites in 2 countries.
Detailed Summary
The purpose of this study was to compare the clinical performance of two different reusable lenses in habitual spherical soft lens wearers.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, United States
CollaboratorsCentre for Ocular Research & Education, Canada
Timeline
N/ACompletedFinished
202420252026
First PostedOct 2023
Enrollment StartNov 2023
Primary CompletionApr 2024
TodayJul 2026
First PostedOct 24, 2023
Enrollment StartNov 13, 2023
Primary CompletionApr 4, 2024
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 2.7 years ago
Interventions
Lens A (fanfilcon A)device
Daily wear for one month
Lens B (lotrafilcon B)device
Daily wear for one month