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Completed Not applicable Interventional Results available

Comparison Between iLux and LipiFlow in the Treatment of Meibomian Gland Dysfunction (MGD): A 12-month, Multicenter Study

ClinicalTrials.gov ID: NCT03956225

Public ClinicalTrials.gov record NCT03956225. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 3:36 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this post-approval study is to demonstrate that iLux treatment offers comparable treatment effectiveness to LipiFlow for MGD treatment at 12 months post single treatment.

Study identification

NCT ID
NCT03956225
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Alcon Research
Industry
Enrollment
299 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 25, 2019 (Actual)
Primary completion
Oct 24, 2020 (Actual)
Completion
Oct 24, 2020 (Actual)
Last update posted
Oct 8, 2021

2019 – 2020

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Alcon Investigator 9083 Long Beach California 90815 —
Alcon Investigator 9081 Los Angeles California 90013 —
Alcon Investigator 9084 San Diego California 92122 —
Alcon Investigator 5127 Panama City Florida 32405 —
Alcon Investigator 4782 Highland Park Illinois 60035 —
Alcon Investigator 6567 Pittsburg Kansas 66762 —
Alcon Investigator 5582 Louisville Kentucky 40206 —
Alcon Investigator 6402 Medina Minnesota 55340 —
Alcon Investigator 1455 Kansas City Missouri 64111 —
Alcon Investigator 3828 Poughkeepsie New York 12603 —
Alcon Investigator 8046 Granville Ohio 43023 —
Alcon Investigator 6313 Powell Ohio 43065 —
Alcon Investigator 9082 Chambersburg Pennsylvania 17201 —
Alcon Investigator 8028 Wichita Falls Texas 76308 —
Alcon Investigator 5163 Kirkland Washington 98034 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03956225, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 8, 2021 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03956225 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →