跳至主要内容
临床试验/NCT03518398
NCT03518398已完成3 期

Effectiveness and Safety of Intense Pulsed Light in Patients With Meibomian Gland Dysfunction

Chulalongkorn University2 个研究点 分布在 1 个国家目标入组 114 人开始时间: 2018年7月3日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
114
试验地点
2
主要终点
Change in fluorescein tear break-up time at month 6 using fluorescein technique

研究概览

简要总结

Meibomian gland dysfunction (MGD) is one of the most common causes of dry eye diseases. Over the past decade, several treatment options in MGD have been extensively studied including warm compression, lid hygiene, ocular lubricants, forceful expression, LipiFlow thermal pulsation system, intraductal probing, debridement scaling and intense pulsed light (IPL). IPL is a broad spectrum, non-coherent and polychromatic light source with a wavelength spectrum of 500-1200 nm. It can be filtered to allow only a range of wavelengths to be emitted. Different wavelength makes different depth of tissue to absorb a specific light energy. Intense pulsed light (IPL) has been widely used in dermatology as a therapeutic tool for removal of hypertrichosis, benign cavernous hemangioma, benign venous malformations, telangiectasia, port-wine stain and pigmented lesions. Concurrent ocular surface improvements have been observed in patients undergone IPL treatment. Very few prospective clinical trials showed that subjective dry eye symptoms decreased and some of the dry eye signs also improved. Nonetheless, there is still inconsistency in the efficacy of IPL among these studies. Biomarkers, specifically cytokines, in dry eye diseases have been studied to some extent. Moreover, the change in ocular surface inflammatory cytokines in patients with MGD after IPL treatment is unclear.

The investigators proposed a prospective randomized double-masked sham-controlled clinical trial to investigate the efficacy and safety of intense pulse light in MGD patients.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Able to read, understand and sign an informed consent form
  • 18-80 years of age
  • Fitzpatrick skin type 1-5
  • Able and willing to comply with the treatment /follow-up schedule and requirements
  • Presence of meibomian gland on each lower eyelid's meibography
  • Current diagnosis of stage1-4 of MGD in both eyes, according to the International Workshop on Meibomian Gland Dysfunction: Report of the Subcommittee on Management and Treatment of Meibomian Gland Dysfunction

排除标准

  • Contact lens wearer within the past 1 month and throughout the study
  • Recent ocular surgery or eyelid surgery within the past 6 months
  • Neuro-paralysis in the planned treatment area within the past 6 months
  • Current use of punctual plugs
  • Pre-cancerous lesions, skin cancer or pigmented lesions in the planned treatment area
  • Uncontrolled infections or uncontrolled immunosuppressive diseases
  • Subjects who have undergone refractive surgery within the past 6 months
  • Diseases in the planned treatment area that could be stimulated by light at 560 nm to 1200 nm (e.g.,Herpes simplex 1 and 2, Systemic Lupus Erythematosus, porphyria)
  • Use of photosensitive medications and/or herbs that may cause sensitivity to 560-1200 nm light exposure, such as isotretinoin, tetracycline, or St. John's Wort
  • Pregnancy and lactation
  • Radiation therapy to the head or neck within the past year, or planned radiation therapy throughout study period
  • Treatment with chemotherapeutic agent within the past 8 weeks, or planned chemotherapy throughout study period
  • Any condition revealed during the eligibility screening process whereby the physician deems the subject inappropriate for this study
  • Declared legally blind in one eye
  • IPL treatment within the past 12 months
  • Lipiflow treatment, or any equivalent treatments, within the past 12 months
  • Any anti-glaucomatous eye drop uses within the past 3 months and throughout the study period

研究组 & 干预措施

IPL group

Experimental

IPL 9-13 J/cm2 according to Fitzpatrick's skin type on day 0, 15, 45

干预措施: Intense Pulsed Light (Device)

IPL group

Experimental

IPL 9-13 J/cm2 according to Fitzpatrick's skin type on day 0, 15, 45

干预措施: Standard treatment (Combination Product)

sham-IPL group

Sham Comparator

IPL 0 J/cm2 according to Fitzpatrick's skin type on day 0, 15, 45

干预措施: Standard treatment (Combination Product)

结局指标

主要结局

Change in fluorescein tear break-up time at month 6 using fluorescein technique

时间窗: day 0, 15, 45, month 3, month 6

time elapsed from the last complete eyelid blink until appearance of the first dry spot on the cornea

次要结局

  • Change in Meibomian gland's anatomy by Meiboscore using Meibography at month 6 using Keratograph 5M (OCULUS, Wetzlar, Germany)(day 0, 15, 45, month 3, month 6)
  • Change in tear osmolarity at month 6 using TearLab Osmolarity System (San Diego, CA)(day 0, 45, month 3, month 6)
  • Change in lipid layer thickness at month 6 using LipiView interferometer (TearScience inc., Morrisville,NC)(day 0, 15, 45, month 3, month 6)
  • Change in dry eye symptoms using Ocular Surface Disease Index (OSDI), a questionnaire, at month 6(day 0, 15, 45, month 3, month 6)
  • Change in Meibomian gland expressibility at month 6 after applying the force onto the eyelids using meibomian gland evaluator(day 0, 15, 45, month 3, month 6)
  • Change in tear production test (Schirmer's test) at month 3 using calibrated strips of a non-toxic filter paper(day 0, month 3)
  • Change in ocular surface staining at month 6 using fluorescein staining technique(day 0, 15, 45, month 3, month 6)
  • Change in Meibum quality at month 6 after applying the force onto the eyelids using meibomian gland evaluator(day 0, 15, 45, month 3, month 6)
  • Change in tear cytokines Interleukins-1 receptor antagonist (IL-1Ra) at month 3 using Bio-Plex® 200 system (Bio-Rad, Hercules, CA)(day 0, month 3)
  • Change in tear cytokines Interleukins-6 at month 3 using Bio-Plex® 200 system (Bio-Rad, Hercules, CA)(day 0, month 3)

研究者

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

Yonrawee Piyacomn, M.D., FICO

Yonrawee Piyacomn, MD, FICO, Principal Investigator, Fellow of Cornea and Refractive Surgery Unit, Department of Ophthalmology, Faculty of Medicine, Chulalongkorn University

Chulalongkorn University

研究点 (2)

Loading locations...

相似试验