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Clinical Evaluation of a Daily Wear Frequent Replacement Silicone Hydrogel Lens

NCT03920280 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2022-07-28

Study results available
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Summary

The purpose of this clinical study is to demonstrate 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.

Conditions

  • Refractive Errors

Interventions

DEVICE

LID015385 contact lenses

Investigational silicone hydrogel contact lenses

DEVICE

Comfilcon A soft contact lenses

Commercially available silicone hydrogel contact lenses

DEVICE

CLEAR CARE

Hydrogen peroxide-based cleaning and disinfecting system

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • CDMA Project 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
2019-05-22
Primary Completion
2019-10-05
Completion
2019-10-05
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 NCT03920280 on ClinicalTrials.gov