MedTrace Logo

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

NCT04476784 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2021-10-26

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to assess the clinical performance of an investigational contact lens over 30 days of daily wear.

Conditions

  • Myopia

Interventions

DEVICE

Lehfilcon A contact lenses

Investigational silicone hydrogel contact lenses

DEVICE

Comfilcon A contact lenses

Commercially available silicone hydrogel 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
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-08-17
Primary Completion
2020-11-18
Completion
2020-11-18
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT04476784 on ClinicalTrials.gov