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Completed Not applicable Interventional Results available

Comparison Between iLux™ and LipiFlow® in the Treatment of Meibomian Gland Dysfunction

ClinicalTrials.gov ID: NCT03055832

Public ClinicalTrials.gov record NCT03055832. 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 21, 2026, 4:27 AM EDT

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

Official title

Randomized Comparison Between iLux™ and LipiFlow® in the Treatment of Meibomian Gland Dysfunction

Brief summary

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

The purpose of this study was to compare changes in meibomian gland dysfunction (MGD), tear break-up time (TBT) and evaporative dry eye (EDE) symptoms after treatment with either the iLux® 2020 System or the LipiFlow® Thermal Pulsation System.

Study identification

NCT ID
NCT03055832
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Tear Film Innovations, Inc.
Industry
Enrollment
142 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
Feb 9, 2017 (Actual)
Primary completion
Jul 20, 2017 (Actual)
Completion
Jul 20, 2017 (Actual)
Last update posted
Apr 12, 2023

2017

United States locations

U.S. sites
7
U.S. states
4
U.S. cities
7
Facility City State ZIP Site status
TearFilm Investigative Site Phoenix Arizona 85016 —
TearFilm Investigative Site Scottsdale Arizona 95260 —
TearFilm Investigative Site San Diego California 92122 —
TearFilm Investigative Site Centennial Colorado 80112 —
TearFilm Investigative Site Greenwood Village Colorado 80111 —
TearFilm Investigative Site Chesterfield Missouri 63017 —
TearFilm Investigative Site Kansas City Missouri 64111 —

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 NCT03055832, 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 Apr 12, 2023 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03055832 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →