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临床试验/NCT01091311
NCT01091311已完成4 期

Phase IV Multicentric Study, 30 Patients Suffering of Meibomian Glands Dysfunction.

Laboratoires Thea6 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2010年5月最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
30
试验地点
6

研究概览

简要总结

Multicentric study, open label, uncontrolled phase IV in 30 patients with meibomian glands dysfunction .

Its objective is to Collect information from patients and ophthalmologists specialized in ocular surface and eyelids to anticipate how Blephasteam ® can be optimized.

This study involves 2 visits, visit of Inclusion, J0, then end of study visit, D21.

Between the two visits patients will be treated with Blephasteam ® for 21 days (up to two uses per day) and complete a questionnaire every two days during the first week and then once a week the next two weeks.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

研究者

申办方类型
Industry

研究点 (6)

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