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临床试验/EUCTR2006-006760-28-AT
EUCTR2006-006760-28-AT进行中(未招募)不适用

Comparision of Ranibizumab (Lucentis) Monotherapy versus Combination of Ranibizumab (Lucentis) with Photodynamic Therapy (Verteporfin) in Patients with Subfoveal Choroidal Neovascularisation due to Age-Related Macular Degeneration - KAV-Ranibizumab

udwig Boltzmann Institut für Retinologie und biomikroskopische Laserchirurgie0 个研究点目标入组 45 人开始时间: 2007年5月30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
45

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

  • The study population will consist of male and female patients > 50 years of age with subfoveal choroidal neovascularization (CNV) secondary to AMD.
  • 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 who have a BCVA of < 33 letters (approximately 20/200) in both eyes
  • ·Prior treatment in the study eye with verteporfin, external-beam radiation therapy, vitrectomy, submacular surgery, other surgical intervention for AMD, or transpupillary thermotherapy
  • ·Previous or current intravitreal drug delivery (e.g., intravitreal corticosteroid injection or device implantation) in the study eye
  • ·Focal laser photocoagulation (juxta-, extra- or subfoveal) in the study eye

研究者

发起方
udwig Boltzmann Institut für Retinologie und biomikroskopische Laserchirurgie

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