Clinical Trials Directory

Trials / Completed

CompletedNCT02958514

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Peking University Third Hospital · Academic / Other
Sex
All
Age
26 Years – 78 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DEVICEintense pulsed lightIntense pulse light (IPL) has been used in dermatology practices for several years as a treatment for rosacea and acne.IPL uses Xenon flashlamp to emit wavelengths of light from 400 to 1200nm. When placed on the light, a filter restricts the wavelength to the visible light range of \*500nm.In 2007-2008, an IPL treatment technology-the Diamond Q4 by DermaMed Solutions-was specifically configured to our specifications with the goal of stimulating secretion of normal meibum via skin treatment effects on the meibomian glands. It was discovered that dry eye patients are better positioned for gland expression, as IPL seems to liquefy the abnormal viscous meibum and dilate the glands.
DRUGTobramycin and Dexamethasone Ophthalmic Ointment

Timeline

Start date
2016-11-01
Primary completion
2017-02-01
Completion
2017-03-01
First posted
2016-11-08
Last updated
2022-05-05

Source: ClinicalTrials.gov record NCT02958514. Inclusion in this directory is not an endorsement.