CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 66 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.

Search/NCT05114564
NCT05114564N/ACompleted

Evaluation of the Performance of Monthly Replacement Sphere Lens Designs in Habitual Soft Contact Lens Wearers

CooperVision, Inc.·interventional·Posted Nov 10, 2021·Updated Apr 4, 2023

In Brief

A clinical study evaluating Lens A (comfilcon A lens) and Lens B (lehfilcon A lens) for Myopia and Hyperopia. Completed, enrolled 66 participants across 4 sites.

Detailed Summary

The objective of the study is to evaluate the clinical performance of two monthly silicone hydrogel contact lenses in habitual wearers of frequent replacement (FRP) lenses when worn for one month.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia, Hyperopia
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20222023202420252026
First PostedNov 10, 2021
Enrollment StartNov 19, 2021
Primary CompletionApr 22, 2022
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 4.6 years ago

Interventions

Lens A (comfilcon A lens)device

1 month

Lens B (lehfilcon A lens)device

1 month