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Evaluation of Wear Experience With a Water Surface Daily Disposable Contact Lens

NCT05102383 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2025-11-25

Study results available
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Summary

The purpose of this study is to assess the wear experience of existing wearers of a monthly replacement contact lens after they have been fit with a daily disposable contact lens that has water surface treatment.

Conditions

  • Contact Lens

Interventions

DEVICE

Comfilcon A Toric contact lenses

Monthly replacement contact lenses

DEVICE

Verofilcon A for Astigmatism Daily Disposable contact lenses

Daily disposable contact lenses

Sponsors & Collaborators

  • Ohio State University

    lead OTHER

Principal Investigators

  • Jennifer Fogt, OD MS · The Ohio State University College of Optometry

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-11-15
Primary Completion
2022-04-19
Completion
2022-04-19
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05102383 on ClinicalTrials.gov