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Clinical Performance Assessment of a Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lens

NCT04055519 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2021-05-13

Study results available
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Summary

The purpose of this study is to obtain on-eye performance data to inform contact lens product development.

Conditions

  • Refractive Errors

Interventions

DEVICE

Lehfilcon A contact lenses

Investigational silicone hydrogel contact lenses

DEVICE

Comfilcon A contact lenses

Commercially available silicone hydrogel contact lenses

DEVICE

Multi-purpose disinfection solution

Solution for cleaning, disinfecting, and reconditioning silicone hydrogel contact lenses

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • CDMA Project Lead, Vision Care · Alcon Research, LLC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-19
Primary Completion
2019-12-03
Completion
2019-12-03
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 NCT04055519 on ClinicalTrials.gov