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临床试验/EUCTR2006-006312-30-HU
EUCTR2006-006312-30-HU进行中(未招募)不适用

A phase IV non-randomized, uncontrolled, open-label, single-center trial to evaluate the safety and efficacy of Macugen (pegaptanib sodium) given by intravitreal injections every 6 weeks in patients with serous pigment epithel detachments (PED) in exudative age-related macular degeneration (AMD)

Dept. of Ophthalmol, Semmelweis University0 个研究点目标入组 30 人开始时间: 2007年1月25日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
30

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

  • Patients of either gender
  • Age: 50 years or above
  • diagnosed with early lesions of serous pigment epithel detachments secondary to AMD
  • Early lesion defined as:
  • best corrected visual acuity >= 20/100,
  • detachments measuring < 6 disc areas
  • absence of any scarring/fibrosis or atrophy within the lesion
  • the absence of subfoveal hemorrhage or total hemorrhage representing greater than 1 disc area
  • 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) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patients with prior treatment with PDT, or subfoveal laser and with clinically significant concomitant diseases will be excluded.

研究者

发起方
Dept. of Ophthalmol, Semmelweis University

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