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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02958514
Other study ID # 2016154
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 2016
Est. completion date March 2017

Study information

Verified date May 2022
Source Peking University Third Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date March 2017
Est. primary completion date February 2017
Accepts healthy volunteers No
Gender All
Age group 26 Years to 78 Years
Eligibility Inclusion Criteria: - patients with dry eye syndrome and diagnosed as MGD Exclusion Criteria: - an infection or inflammatory disease; - ocular surgical history with in the last 3 months - SGOGREN SYNDROME

Study Design


Intervention

Device:
intense pulsed light
Intense 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.
Drug:
Tobramycin and Dexamethasone Ophthalmic Ointment


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Peking University Third Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Ocular Surface Disease Index (OSDI) normal value:<13 abnormal value:= 13 through study completion,an average of 6 months
Secondary The concentrations of inflammatory cytokines such as IL-1?IL-6 and IL-8 through study completion,an average of 6 months
Secondary breakup time of tear film (BUT) normal value:>10s abnormal value:= 10s through study completion,an average of 6 months
Secondary Corneal Fluorescein Stain(CFS) through study completion,an average of 6 months
Secondary Eyelid ester discharge ability score through study completion,an average of 6 months
Secondary Eyelid ester trait ratings through study completion,an average of 6 months
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