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临床试验/NCT07329712
NCT07329712招募中不适用

Comparing Tear Proteomics Profile in Dry Eye Disease pre-and Post-treatment With Low Level Light Therapy

Singapore National Eye Centre1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年11月5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
30
试验地点
1
主要终点
Comparing tear proteomics profile in dry eye disease pre-and post-treatment with low level light therapy

研究概览

简要总结

The purpose of this research study is to understand the mechanism of action of low level light therapy and also potentially yield markers associated with good treatment response. Low-level light therapy is light-based treatment delivered through advance eye-light device. This therapy uses light energy to provide energy to the meibomian gland cells to slow down age-ing, improve tear stability and reduce inflammation.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

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

入选标准

  • Must be eligible for, and have consented for low level light therapy
  • Must not have presented to the clinic for an acute eye problem such as visual loss or painful eye
  • Ability to give informed consent.
  • Age more or equals to 21 years old.

排除标准

  • Patients who are unable to or decline to give consent.
  • Age less than 21 years old.
  • Patients who presented to the clinic for an acute eye problem such as visual loss or painful eye.
  • Patients not suitable for low level lighttherapy:
  • Fitted with pacemakers, metal, electrical, acoustic prosthetics
  • Epilepsy, cardiac rhythm or frequency disorders
  • Fever, thrombophlebitis or acute phlebitis of the legs, large-sized varicose veins, or venous surgery within 2 months
  • Uncontrolled hypertension or severe diabetes
  • Open wounds on eyelid or skin
  • Evolving cancer or hepatitis
  • Blood anticoagulant or coagulation defect

研究组 & 干预措施

Patients undergoing low level light therapy

结局指标

主要结局

Comparing tear proteomics profile in dry eye disease pre-and post-treatment with low level light therapy

时间窗: Baseline visit and Post Baseline visit 3 months (+3 weeks).

Aim 1: Tear proteomic profile of MGD patients with DED pre- and post-treatment with LLLT will be profiled Aim 2: Baseline tear cytokine levels will be measured using the novel Olink 500-plex technology in DED patients with MGD undergoing LLLT

次要结局

未报告次要终点

研究者

申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Louis Tong

Clinician-Scientist, Senior Consultant

Singapore National Eye Centre

研究点 (1)

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