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Meibomian Gland Dysfunction clinical trials

View clinical trials related to Meibomian Gland Dysfunction.

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NCT ID: NCT03265652 Completed - Dry Eye Clinical Trials

IPL and MGX Versus MGX Alone in the Treatment of Dry Eye Disease Secondary to MGD

Start date: May 15, 2018
Phase: N/A
Study type: Interventional

The aim of the current study is to examine the contribution of intense pulsed light (IPL) for relieving signs and symptoms of dry eye due to meibomian gland dysfunction. The effect of IPL will be examined in a study designed as a randomized controlled trial. In the study arm, subjects will undergo 4 treatment sessions, consisting of IPL pulses immediately followed by expression of the meibomian glands. In the control arm, subjects will undergo the same treatments, except that the IPL pulses will be disabled. For each subject, the duration of the study will be 10 weeks, as explained in the detailed description,

NCT ID: NCT03162497 Recruiting - Dry Eye Syndromes Clinical Trials

Effect of Topical Azithromycin on Tear Film Thickness in Patients With Meibomian Gland Dysfunction

Start date: January 8, 2018
Phase: Phase 4
Study type: Interventional

Meibomian gland dysfunction (MGD) is among the leading causes for dry eye syndrome (DES), affecting millions of people worldwide. We have shown in a previous study that tear film thickness (TFT) is reduced in patients with DES and that this reduction correlates with tear break up time (BUT) as well as with the severity of subjective symptoms. Even though systemic tetracyclines as well as topical azithromycin can be used for the treatment of MGD, it seems that topical azithromycin is more effective than tetracyclines and also has the advantage of better tolerability. The hypothesis of the present study is that topical treatment with azithromycin leads to a more pronounced increase in TFT compared to oral doxycycline in patients with DES caused by MGD. The objective of this study is to compare the effect of treatment with topical azithromycin or oral doxycycline on tear film thickness in patients with DES caused by MGD.

NCT ID: NCT03060005 Recruiting - Clinical trials for Meibomian Gland Dysfunction

Is Sjögren's Syndrome Associated With Meibomian Gland Dysfunction ?

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

The investigators hypothesize that the dry eye caused by SS may include the evaporative type, resulting from the MGD. Furthermore, the investigators hypothesize that both pSS and sSS are associated with MGD.To test our hypothesis, we conducted a prospective clinical study in patients with SS (both pSS and sSS) and MGD, and the normal population All subjects were matched for both age and gender and assessed for tear function and ocular surface signs and symptoms.

NCT ID: NCT03055897 Completed - Clinical trials for Meibomian Gland Dysfunction

Tear Film Innovations iLux Safety Study

Start date: May 3, 2016
Phase: N/A
Study type: Interventional

The objective of this study was to measure the temperature of the cornea and surrounding eye tissue temperature immediately after heating the eyelids with the iLux device using the protocol treatment profile. Eligible participants attended one treatment visit, with follow-up one day following the procedure.

NCT ID: NCT03055832 Completed - Clinical trials for Meibomian Gland Dysfunction

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

Start date: February 9, 2017
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT03012698 Completed - Dry Eye Clinical Trials

Pilot Study for Testing Safety of Repetitive Magnetic Stimulation for Treatment of Dry Eye

Start date: November 1, 2017
Phase: N/A
Study type: Interventional

The study aims to test the safety of Repetitive Magnetic Stimulation (RMS) treatment for dry eye disease. Patients are asked to undergo a one-time treatment with Epitech Ocular Magnetic Stimulation Device on one eye in the first stage and both eyes sequentially in the second stage of the study. Changes are monitored for over a study period of 3 months.

NCT ID: NCT02975557 Terminated - Dry Eye Clinical Trials

Brimonidine Eye Drops for Treatment of Ocular Graft-vs-Host Disease (oGVHD)

Start date: May 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The objective of this study is to establish whether patients with dry eye disease (DED) are able to tolerate receiving Brimonidine: 0.15% eye drops two times a day for twelve weeks (primary tolerability objective) and to investigate the preliminary efficacy of Brimonidine 0.15% topical eye drop solution in treating Meibomian Gland Dysfunction (MGD) (primary efficacy objective). Meibomian Gland dysfunction can happen with numerous conditions such as Rosacea, Sjögren's syndrome, and oGVHD. In order to limit the influence of differing etiologies on the outcome of this trial, the investigator has limited the screening to MGD that accompanies oGVHD.

NCT ID: NCT02958514 Completed - Dry Eye Syndrome Clinical Trials

Efficacy Comparison of Two Kinds of Treatment in Treating Dry Eye Caused by Meibomian Gland Dysfunction

Start date: November 2016
Phase: N/A
Study type: Interventional

This study aims to evaluate the efficacy of intense pulsed light in treating dry eye caused by meibomian gland dysfunction and make a comparison between the traditional treatment.

NCT ID: NCT02956083 Completed - Dry Eye Syndromes Clinical Trials

The Effect of Tear Supplements on Contact Lens Comfort

Start date: July 2014
Phase: N/A
Study type: Interventional

The primary goal of this investigation is to determine if lipid based artificial tear supplementation has an impact on contact lens discomfort (CLD).

NCT ID: NCT02952079 Completed - Dry Eye Clinical Trials

Comparison of BlephEx to MiBoflo as Treatment Options for Blepharitis

Start date: May 2015
Phase: N/A
Study type: Interventional

The goal of this study is to compare which treatment - BlephEx or MiBoFlo - will be a better option for patients suffering from dry eye secondary to Meibomian Gland dysfunction.