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Clinical Performance Assessment of Two Silicone Hydrogel Daily Disposable Contact Lenses

NCT05725317 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 114

Last updated 2024-08-06

Study results available
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Summary

The purpose of this study is to assess the overall clinical performance of a contact lens made with a modified manufacturing process.

Conditions

  • Refractive Errors
  • Myopia

Interventions

DEVICE

LID220365 contact lens

Investigational delefilcon A spherical contact lens made with a modified manufacturing process

DEVICE

LID006961 contact lens

Commercially available delefilcon A spherical contact lens

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
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-02
Primary Completion
2023-06-27
Completion
2023-06-27
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 NCT05725317 on ClinicalTrials.gov