跳至主要内容
临床试验/NCT04115800
NCT04115800已完成早期 1 期

Subconjunctival Treatment of Liposomal Sirolimus as a Treatment for Dry Eye Disease

Instituto de Oftalmología Fundación Conde de Valenciana1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2019年10月2日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
发起方
入组人数
52
试验地点
1
主要终点
Ocular Surface Disease Index (OSDI)

研究概览

简要总结

Dry eye disease is a very frequent pathology that importantly affects the quality of life of patients; in spite of the common use of eye lubricants to ameliorate symptoms, there is still a large number of patients who do not present improvement of the disease or they worsen. Although its etiology is varied, the imbalance of the immune system plays a substantial role in the development of dry eye disease. Rapamycin or sirolimus is an anti-inflammatory and immunomodulatory drug that has an enormous potential in ocular surface pathologies such as dry eye disease. The aim of the present study is to determine the effectiveness and security of subconjunctival application of a new formulated drug of liposomal sirolimus in patients with moderate and severe dry eye disease. This is a randomized placebo-controlled double blind clinical trial. Patients presenting data of moderate or severe dry eye disease will be randomized into two groups. One group will receive additional to the conventional treatment, subconjunctival injections of liposomal sirolimus; meanwhile the other group will receive subconjunctival placebo injections. After intervention the effectiveness and the security of the liposomal sirolimus will be evaluated.

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, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects with moderate or severe Dry Eye
  • Subjects with OSDI score > 22
  • Subjects with Van Bijsterveld staining score >4
  • Subjects that accept to participate in the study

排除标准

  • Subjects with refraction surgery antecedents
  • Subjects with ophthalmic surgery six months previous to the study
  • Subjects with Lagophthalmos
  • Subjects with facial paralysis antecedents
  • Subjects with herpetic keratitis
  • Subjects using isotretinoin
  • Pregnant subjects
  • Subjects in lactating period
  • Subjects with allergy or intolerant to the drug
  • Subjects with hepatic disorders
  • Subjects with abnormal thoracic X rays

研究组 & 干预措施

Liposomal Sirolimus

Experimental

Subconjunctival injections of liposomal sirolimus in patients with conventional treatment with moderate and severe dry deye disease

干预措施: Liposomal Sirolimus (Drug)

Liposomal

Placebo Comparator

Subconjunctival liposomal injections in patients with conventional treatments and moderate and severe dry eye disease

干预措施: Liposomal Sirolimus (Drug)

结局指标

主要结局

Ocular Surface Disease Index (OSDI)

时间窗: Six weeks after intervention

The OSDI is assessed on a scale of 0 to 100, with higher scores representing greater disability. The index demonstrates sensitivity and specificity in distinguishing between normal patients and patients with dry eye disease. The OSDI is a valid and reliable instrument for measuring dry eye disease severity (normal, mild to moderate, and sever) and effect on vision -related function.

次要结局

未报告次要终点

研究者

发起方
Instituto de Oftalmología Fundación Conde de Valenciana
申办方类型
Other
责任方
Sponsor

研究点 (1)

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