Clinical Comparison of Two Daily Disposable Contact Lenses - Pilot Study 3

NCT04942925 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2022-09-07

Study results available
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Summary

The purpose of this study is to evaluate the overall performance of PRECISION1™ contact lenses when compared to INFUSE™ contact lenses.

Conditions

  • Myopia
  • Ametropia

Interventions

DEVICE

Verofilcon A contact lenses

Commercially available silicone hydrogel contact lenses for daily disposable wear

DEVICE

Kalifilcon A contact lenses

Commercially available silicone hydrogel contact lenses for daily disposable wear

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Clinical Trial Lead, Vision Care · Alcon Research, LLC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-07-20
Primary Completion
2021-09-09
Completion
2021-09-09
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 NCT04942925 on ClinicalTrials.gov