CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 81 enrolled
Drug / intervention
Deseyne Daily Disposable Contact Lens (Test Device)device
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/NCT05927753
NCT05927753N/ACompleted
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A Randomized, Active-Controlled, Open-Label Study to Evaluate the Clinical Performance of Deseyne (Vifilcon C) Daily Disposable Soft Contact Lens

Bruno Vision Care·interventional·Posted Jul 3, 2023·Updated Oct 2, 2025

In Brief

A clinical study evaluating Deseyne Daily Disposable Contact Lens (Test Device) for Refractive Error - Myopia Bilateral. Completed, enrolled 81 participants across 3 sites.

Detailed Summary

This clinical study is to provide clinical performance data comparing the test lens (Deseyne \[vifilcon C\] daily disposable soft contact lens) to a control lens (1-Day Acuvue Moist \[etafilcon A\] daily disposable soft contact lens) in the same indication for use (single use prior to removal followed by a fresh lens upon the next lens wear exposure). The study is designed to test the hypothesis that the test lens is substantially equivalent to the control lens in like indications for use.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRefractive Error - Myopia Bilateral
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
202420252026
First PostedJul 3, 2023
Enrollment StartJun 8, 2023
Primary CompletionJan 8, 2024
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 3.0 years ago

Interventions

Deseyne Daily Disposable Contact Lens (Test Device)device

Comparison of contact lens performance between the test lens under study (Deseyne Daily Disposable Contact Lens) and the control lens f(1-Day Acuvue Moist Contact Lens) for safety and effectiveness.