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Clinical Evaluation of a Daily Wear Silicone Hydrogel Lens

NCT04207749 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 249

Last updated 2022-02-02

Study results available
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Summary

The purpose of this clinical study is to assess the safety and performance of an investigational soft contact lens compared to a commercially available soft contact lens when worn in a daily wear modality with frequent replacement.

Conditions

  • Refractive Errors
  • Myopia
  • Hyperopia

Interventions

DEVICE

LID015385 contact lenses

Investigational soft contact lenses

DEVICE

Comfilcon A contact lenses

Commercially available soft contact lenses

DEVICE

CLEAR CARE

Hydrogen peroxide-based cleaning and disinfecting solution

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Sr. Clinical Trial Lead, CDMA 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
2020-01-22
Primary Completion
2020-12-17
Completion
2020-12-17
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 NCT04207749 on ClinicalTrials.gov