MGD: Therapeutic Effectiveness of Different Machines in Intense Pulsed Light Treatment of Meibomian Gland Dysfunction

Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University (Other)
Overall Status
Completed
CT.gov ID
NCT06034626
Collaborator
Aier Eye Hospital, Wuhan (Other)
216
3
2
13.4
72
5.4

Study Details

Study Description

Brief Summary

This study aimed to determine the therapeutic effectiveness of different machines in intense pulsed light (IPL) treatment of meibomian gland dysfunction (MGD). Subjects diagnosed with MGD underwent three sessions of IPL treatment in a control (M22) treatment group or experimental (OPL-I) treatment group and were followed up three to four weeks after each session. Tear breakup time (TBUT), meibomian gland secretion scores (MGSS), meibomian gland meibum scores (MGMS), corneal fluorescein staining (CFS) scores, and the Standard Patient Evaluation of Eye Dryness (SPEED) was used to assess eye dryness signs and symptoms at baseline and follow-up visits.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Intense pulsed light
  • Drug: 0.3% hyaluronic acid eye drops
Phase 3

Study Design

Study Type:
Interventional
Actual Enrollment :
216 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The trial aimed to assess therapeutic effectiveness of the study treatment arm (OPL-I with the dual filter system; Miracle Laser systems, Wuhan, China) to the control treatment arm (M22 with a single filter; Lumenis, Yokneam, Israel). Each MGD patient underwent three treatment sessions at three-week intervals and three follow-up examinations over the course of treatment.The trial aimed to assess therapeutic effectiveness of the study treatment arm (OPL-I with the dual filter system; Miracle Laser systems, Wuhan, China) to the control treatment arm (M22 with a single filter; Lumenis, Yokneam, Israel). Each MGD patient underwent three treatment sessions at three-week intervals and three follow-up examinations over the course of treatment.
Masking:
Single (Participant)
Masking Description:
Patients receiving IPL treatment were masked.
Primary Purpose:
Treatment
Official Title:
Therapeutic Effectiveness of Different Machines in Intense Pulsed Light Treatment of Meibomian Gland Dysfunction
Actual Study Start Date :
Nov 3, 2020
Actual Primary Completion Date :
Aug 10, 2021
Actual Study Completion Date :
Dec 15, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: OPL-I

Patients treated with OPL-I with the dual filter system

Procedure: Intense pulsed light
Each MGD patient underwent three treatment sessions at three-week intervals and three follow-up examinations over the course of treatment.

Drug: 0.3% hyaluronic acid eye drops
0.3% hyaluronic acid eye drops (Hialid; Santen, Osaka, Japan) four times a day during the study, including the follow-up period.

Active Comparator: M22

Patients treated with OPL-I with the single filter system

Procedure: Intense pulsed light
Each MGD patient underwent three treatment sessions at three-week intervals and three follow-up examinations over the course of treatment.

Drug: 0.3% hyaluronic acid eye drops
0.3% hyaluronic acid eye drops (Hialid; Santen, Osaka, Japan) four times a day during the study, including the follow-up period.

Outcome Measures

Primary Outcome Measures

  1. SPEED Scores [Baseline, 1 month, 2 months, 3 months, 4 months]

    Standard Patient Evaluation of Eye Dryness questionnaire

  2. CFS scores [Baseline, 1 month, 2 months, 3 months, 4 months]

    corneal fluorescein staining scores

  3. TBUT [Baseline, 1 month, 2 months, 3 months, 4 months]

    Tear breakup time

  4. MGSS [Baseline, 1 month, 2 months, 3 months, 4 months]

    Meibomian gland secretion scores. The MGSS evaluates the obstruction of meibum along the lower eyelid. Three positions along the lower eyelid were detected (five nasal, five central, and five temporal meibomian glands). A score of 0 indicated secretion by all five glands, a score of 1 indicated secretion by three to four glands, a score of 2 indicated secretion by one or two glands, and a score of 3 indicated no secretion by any glands.

  5. MGMS [Baseline, 1 month, 2 months, 3 months, 4 months]

    meibomian gland meibum scores. The MGMS evaluates the quality of meibum along the lower eyelid, with a score of 0 indicating clear liquid meibum, a score of 1 indicating cloudy liquid meibum, a score of 2 indicating cloudy granular meibum, and a score of 3 indicating toothpaste-like solid meibum).

Secondary Outcome Measures

  1. BCVA [Baseline, 4 months]

    best-corrected visual acuity

  2. IOP [Baseline, 4 months]

    intraocular pressure measurements

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Fitzpatrick skin type I-IV according to sun sensitivity and skin appearance

  2. A Standard Patient Evaluation of Eye Dryness (SPEED) score of ≥6

  3. Tear breakup time (TBUT) of ≤10 s in the studied eye

  4. Corneal fluorescein staining (CFS) score of ≥1 (it is not necessary to consider this criterion if the TBUT is ≤5 s)

  5. Meibomian gland secretion score (MGSS) of ≥6 in the studied eye.

Exclusion Criteria:
  1. Use of prescription eye drops (excluding artificial tears) within 48 hours of recruitment

  2. Facial IPL treatment within the prior 12 months

  3. Any surgery of the eye or eyelids within the prior six months

  4. Ocular surface and eyelid abnormalities

  5. Any systemic condition that might cause eye dryness

  6. Use of photosensitive drugs within the prior three months

  7. Precancerous lesions

  8. Skin cancer or pigmented lesions in the treatment area

  9. Overexposure to the sun within the previous month

  10. Ocular infections within the previous six months

  11. Uncontrolled infections or immunosuppressive diseases

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hankou Aier Eye Hospital, Wuhan,Hubei Province Wuhan Hubei China 430000
2 Wuhan Aier Eye Hospital, Wuhan,Hubei Province Wuhan Hubei China 430000
3 2nd Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang China 310000

Sponsors and Collaborators

  • Second Affiliated Hospital, School of Medicine, Zhejiang University
  • Aier Eye Hospital, Wuhan

Investigators

  • Study Director: Xiuming Jin, PhD, Eye Center of the 2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Second Affiliated Hospital, School of Medicine, Zhejiang University
ClinicalTrials.gov Identifier:
NCT06034626
Other Study ID Numbers:
  • 2020-210
First Posted:
Sep 13, 2023
Last Update Posted:
Sep 13, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Second Affiliated Hospital, School of Medicine, Zhejiang University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 13, 2023