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Clinical Comparison of Two Daily Disposable Toric Soft Contact Lenses

NCT05483127 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 153

Last updated 2023-11-02

Study results available
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Summary

The primary purpose of this study is to demonstrate noninferiority in the visual acuity at distance when wearing PRECISION1™ for Astigmatism (P1fA) soft contact lenses compared to another commercially available, soft toric contact lens, MyDay® toric (MDT).

Conditions

  • Astigmatism
  • Ametropia
  • Myopia

Interventions

DEVICE

Verofilcon A toric soft contact lenses

Soft contact lenses for optical correction of ametropia and astigmatism

DEVICE

Stenfilcon A toric soft contact lenses

Soft contact lenses for optical correction of ametropia and astigmatism

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Sr. 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
2022-09-13
Primary Completion
2022-10-31
Completion
2022-10-31
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 NCT05483127 on ClinicalTrials.gov