EUCTR2006-004367-57-AT进行中(未招募)1 期
Treatment of retinal angiomatous proliferation lesions due to age-related macular degeneration with ranibizumab (Lucentis®) and photodynamic therapy with verteporfin (Visudyne®) - LUPRA
Department of Ophthalmology, Medical University of Graz0 个研究点目标入组 15 人开始时间: 2008年4月7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
- 15
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 who at baseline
- •have a best corrected visual acuity (BCVA) letter score in the study eye between 73-24 (approximately 20/40 to 20/320) using an ETDRS chart measured at 4 meters or Snellen equivalent
- •have a RAP lesion in the study eye with the following characteristics as determined by fluorescein and indocyanine green angiography:
- •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
- •any other form of AMD or of neovascular maculopathy, including pathologic myopia, angioid streaks, infectious or inflammatory chorioretinal diseases, ocular tumors, prior radiation therapy, hereditary disorders, or trauma.
- •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
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