Intense Pulsed Light in Meibomian Gland Dysfunction

Sponsor
Prim. Prof. Dr. Oliver Findl, MBA (Other)
Overall Status
Recruiting
CT.gov ID
NCT05089591
Collaborator
(none)
38
1
2
12.4
3.1

Study Details

Study Description

Brief Summary

Meibomian gland dysfunction (MGD) is a major cause of dry eye disease (DED). Up to 86% of patients suffering from DED also show signs of MGD. Traditional treatment of MGD is based on eye lid hygiene and massage in combination with intensive usage of lubricants.

Recently, a novel technology the intense pulsed light (IPL) therapy was introduced, which shows promising results in patients with meibomian gland dysfunction. Originating from field of dermatology, subjecting improvement of dry eye symptoms was recognized after the treatment of facial rosacea using IPL. Different hypotheses exist how IPL treatment might improve the situation in the dry eye patient. Warming of the eyelid, due to the light application and reduction of bacterial load are two possible mode of actions. Further, the used wavelengths in IPL may be modified that the light is only absorbed by oxygenated haemoglobin, which lead to an obliteration of telangiectasia and reduced inflammation on the lid margin. This principal is applied in the treatment of facial rosacea.

Aim of this study is to investigate the effect of IPL therapy in patients with MGD on dry eye parameters as well as subjective complaints.

Condition or Disease Intervention/Treatment Phase
  • Device: Intense Pulsed Light therapy
  • Device: Sham Treatment
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
38 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Bilateral comparisonBilateral comparison
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Efficacy of Intense Pulsed Light Treatment in Patients With Meibomian Gland Dysfunction
Actual Study Start Date :
Oct 20, 2021
Anticipated Primary Completion Date :
Oct 20, 2022
Anticipated Study Completion Date :
Nov 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Study eyes

Study eye receives the standard energy dose as recommended by the manufacturer (between 8 and 12J/cm2, in accordance with the manufacturer's recommendations).

Device: Intense Pulsed Light therapy
The LacryStim System is a CE marked device for treatment of meibomian gland dysfunction. It stimulates and reactivates meibomian glands and improves the related dry eye condition. Intense pulsed light is emitted with a light spectrum from 610nm to 1200nm. Each treatment consists of short individual pulses lasting for 4ms separated by a 26ms lasting interval to hinder tissue temperature increase, thermal damage to the skin and inflammatory reaction. During this phase 8 to 12 J / cm2 are delivered. Selection of total energy levels depends on the skin type (Fitzpatrick Skin Types) as recommended by the manufacturer.

Sham Comparator: Control eyes

The control eye is treated using low energy dose energy (1J/ cm2) as sham treatment, ensuring blinding of the respective patient.

Device: Sham Treatment
The fellow eye serves as the control eye. Study eye receives the standard energy dose as recommended by the manufacturer (between 8 and 12J/cm2, in accordance with the manufacturer's recommendations). The control eye is treated using low energy dose energy (1J/ cm2) as sham treatment, ensuring blinding of the respective patient.

Outcome Measures

Primary Outcome Measures

  1. Difference Meibum quality score and expressibility between both eyes during the 6-month visit [6-months visit]

Secondary Outcome Measures

  1. Comparison of dry eye related parameters between both eyes (tear film break up time, Oxford Staining) [6 months]

  2. Change of dry eye related parameters during the study period in the study eye (tear film break up time, Oxford Staining) [6 months]

  3. Change of Ocular Surface Disease Index (OSDI) score during the study period [6 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age older than 18 years

  • Presence of meibomian gland dysfunction at any stage

  • Presence of meibomian glands on each lower eyelid's Meibography

Exclusion Criteria:
  • Fitzpatrick Skin Type VI

  • Usage of eye drops other than lubricants (e.g. antibiotics, steroids, cyclosporin-A)

  • Usage of systemic antibiotic therapy

  • Any pathology of the ocular surface except dry eye disease (e.g. corneal scarring, cornea ectasia)

  • Ocular surgery within prior 3 months

  • Ocular injury within prior 3 months

  • Ocular herpes of eye or eyelid within prior 3 months

  • Active ocular infection

  • Active ocular inflammation or history of chronic, recurrent ocular inflammation within prior 3 months

  • Eyelid abnormalities that affect lid function

  • Ocular surface abnormality that may compromise corneal integrity

  • Pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Vienna Institute for Research in Ocular Surgery Vienna Austria 1140

Sponsors and Collaborators

  • Prim. Prof. Dr. Oliver Findl, MBA

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Prim. Prof. Dr. Oliver Findl, MBA, Prim. Univ. Prof. Dr. Oliver Findl, MBA, Vienna Institute for Research in Ocular Surgery
ClinicalTrials.gov Identifier:
NCT05089591
Other Study ID Numbers:
  • IPL
First Posted:
Oct 22, 2021
Last Update Posted:
Oct 22, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 22, 2021