跳至主要内容
临床试验/NCT06468930
NCT06468930招募中不适用

Efficacy of Adjunctive Low-Level Light Therapy to Intense Pulsed Light for Meibomian Gland Dysfunction

Chulalongkorn University2 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2024年10月2日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
58
试验地点
2
主要终点
Lipid layer thickness (LLT)

研究概览

简要总结

The goal of this clinical trial is to compare the effectiveness of adjunctive low-level light therapy (LLLT) to intense pulsed light (IPL) versus intense pulsed light (IPL) alone for the treatment of meibomian gland dysfunction (MGD).

The main question it aims to answer is does the adjunctive of low-level light therapy (LLLT) to intense pulsed light (IPL) provide more beneficial treatment effects than intense pulsed light (IPL) alone in treating meibomian gland dysfunction (MGD) patients?

Participants will be randomized into 2 groups: adjunctive low-level light therapy (LLLT) to intense pulsed light (IPL) group (ALLLT +IPL) and IPL alone group.

详细描述

In both the IPL group and the ALLLT+IPL group, the doctor will administer IPL therapy to each participant and apply the Light Modulation® special facial mask to their faces. The assistant nurse will activate the light power, ensuring that the doctor remains blind to treatment allocation. Participants in both groups will receive a conventional treatment for MGD including warm compression and lid hygiene. Moreover, all participants will be advised to use preservative-free artificial tears 4 times daily throughout the study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • History of previous ocular trauma or surgery within the past six months
  • Contact lens-wearing patients
  • Patients with skin-pigmented lesions in the treatment area
  • Pregnancy or breastfeeding patients
  • Patients with any uncontrolled ocular or systemic diseases

结局指标

主要结局

Lipid layer thickness (LLT)

时间窗: baseline, 2 weeks, 4 weeks, 12 weeks, and 24 weeks post treatment

Lipid layer thickness will be evaluated using Lipiview® II interferometer (TearScience®, Johnson \& Johnson Vision, California, USA). The thickness of the lipid layer is then calculated from the interference pattern and expressed in interferometric color units (ICU), where 1 ICU reflects approximately 1 nm of lipid layer thickness.

次要结局

  • Meibum quality score(baseline, 2 weeks, 4 weeks, 12 weeks, and 24 weeks post treatment)
  • Tear film break-up time (TBUT)(baseline, 2 weeks, 4 weeks, 12 weeks, and 24 weeks post treatment)
  • Meibum expressibility score(baseline, 2 weeks, 4 weeks, 12 weeks, and 24 weeks post treatment)
  • Meiboscore(baseline, 2 weeks, 4 weeks, 12 weeks, and 24 weeks post treatment)
  • Conjunctival and corneal staining:(baseline, 2 weeks, 4 weeks, 12 weeks, and 24 weeks post treatment)
  • Ocular surface disease index (OSDI) scores(baseline, 2 weeks, 4 weeks, 12 weeks, and 24 weeks post treatment)
  • Tear cytokines levels(baseline and 12 weeks post treatment)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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