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临床试验/EUCTR2009-009998-10-DE
EUCTR2009-009998-10-DE进行中(未招募)1 期

Myfortic (enteric-coated mycophenolate sodium) for the treatment of non-infectous intermediate uveitis – a prospective, controlled randomized multicenter trial

Centre for Ophthalmology, University of Tuebingen0 个研究点目标入组 144 人开始时间: 2009年12月2日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
144

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Subjects with a documented at least 6 months history of unilateral or bilateral intermediate uveitis either idiopathic or due to non-infectious systemic disease (e.g. sarcoidosis, multiple sclerosis);
  • Uveitis has to be considered to be active at the timeoint of enrolment according to at least one of the following criteria:
  • oGrade 2+ or higher for vitreous haze
  • oGrade 2+ or higher for anterior chamber cells
  • oPresence of cystoid macular edema in OCT
  • oPresence of retinal vessel leakage in FA
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Uveitis of infectious etiology
  • Clinically suspected or confirmed central nervous system or ocular lymphoma
  • Primary diagnosis of anterior or posterior uveitis

研究者

发起方
Centre for Ophthalmology, University of Tuebingen

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