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临床试验/NCT05594745
NCT05594745已完成4 期

Comparative Efficacy of Different Treatment Regimens in Patients With Dry Eye Disease and Meibomian Gland Dysfunction

Tauber Eye Center1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年3月2日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
60
试验地点
1
主要终点
eye dryness score

研究概览

简要总结

This study seeks to explore the relevance of inflammation in dry eye patients with MGD and compare the efficacy of LipiFlow treatment followed by lid hygiene and lubricant treatment with Systane Ultra or LipiFlow treatment followed by lid hygiene and lifitegrast treatment in patients with meibomian gland dysfunction.

详细描述

The role of inflammation as a central mechanism of pathophysiology in dry eye disease has been well documented, including both clinical and basic science studies. It has been estimated that 50-75% of patients complaining of dry eyes have meibomian gland dysfunction (MGD). As defined by TFOS DEWs II MGD is a chronic, diffuse abnormality of the meibomian glands, commonly characterized by terminal duct obstruction and/or qualitative/quantitative changes in the glandular secretion. This may result in the alteration of the tear film, symptoms of eye irritation, clinically apparent inflammation, and ocular surface disease. It has been estimated that 86% of patients complaining of dry eye disease demonstrate meibomian gland dysfunction. The role of ocular surface inflammation vs. the role of obstructive meibomian gland disease is less well understood.

The symptoms of MGD (evaporative dry eye) may be difficult to differentiate from those of dry eye syndrome (aqueous deficient dry eye (ADDE)), though MGD patients tend to report more burning and stinging than they report complaints of grittiness, sandiness or foreign body sensation in the eyes. However, there is a significant lack of association between signs and symptoms in patients with dry eye disease, which makes it extremely difficult to sort out which patients would benefit from which treatment options. Given the high prevalence of dry eye in the general population any attempt to segregate patients into appropriate treatment types is important.

Traditional treatment options for MGD include the use of artificial lubricants (some lipid-containing such as Systane Ultra), warm lid compresses using cloths or heat pads of various materials, systemic tetracyclines and episodic treatment with topical antibiotics or antibiotic/steroid combinations. Eyelid thermal pulsation procedures (e.g. LipiFlow) have helped many patients. Only one published study supports the benefit of anti-inflammatory treatment (lifitegrast) in patients with MGD. This study seeks to explore the relevance of inflammation in dry eye patients with MGD and compare the efficacy of LipiFlow treatment followed by lid hygiene and lubricant treatment with Systane Ultra or LipiFlow treatment followed by lid hygiene and lifitegrast treatment in patients with meibomian gland dysfunction.

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
Single (Investigator)

盲法说明

Randomized

入排标准

性别
All
接受健康志愿者

入选标准

  • Adult patients aged 18 or older, of any sex and any race.
  • Clinical diagnosis of MGD, defined as:
  • complaints of burning, stinging or dryness > 40 on scale of 0-
  • thickened secretions or occlusion of > 4 of eight assessed glands of the central lower eyelid.
  • clinically evident redness of the eyelid margin > 1+ on a scale of 0-
  • Willing to comply with the protocol instructions.
  • Has read (or has had read to), understood, and signed an Informed Consent.

排除标准

  • Active ocular infection or ocular inflammatory disease.
  • Anterior basement membrane dystrophy or history of recurrent erosion syndrome.
  • History of severe / serious ocular pathology or other medical condition that could result in an inability to safely complete the study.
  • Ocular surgery, LipiFlow or iLux or IPL or MG duct probing within past 6 months.
  • Participation by the patient in any other investigational study within the past 30 days.
  • Unlikely to comply with protocol instructions for any reason (confusion, substance abuse, etc.).
  • The Principal Investigator or the Medical Monitor reserves the right to declare a patient ineligible based on medical evidence that indicates the patient is unsuitable for the study.

研究组 & 干预措施

Systane

Active Comparator

One drop QID for 9 months

干预措施: Lipiflow (Device)

Xiidra

Active Comparator

one drop BID for 9 months

干预措施: Lifitegrast Ophthalmic (Drug)

Xiidra

Active Comparator

one drop BID for 9 months

干预措施: Lipiflow (Device)

Systane

Active Comparator

One drop QID for 9 months

干预措施: Systane Free (Drug)

结局指标

主要结局

eye dryness score

时间窗: 9 months

visual analog scale from 0 to 100, higher is worse

次要结局

  • corneal flurescein staining(9 months)
  • ocular discomfort score(9 months)

研究者

发起方
Tauber Eye Center
申办方类型
Other
责任方
Principal Investigator
主要研究者

Joseph Tauber

Principal Investigator

Tauber Eye Center

研究点 (1)

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