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临床试验/JPRN-UMIN000012013
JPRN-UMIN000012013已完成未知

The Correlation for Improvement of Visual Acuity and QOL after Ranibizumab Treatment for Age-Related Macular Degeneration Patients - QUATRO Study

Clinical Research Support Center Kyushu0 个研究点目标入组 100 人开始时间: 2013年11月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
50years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Patients whose lesion site evaluated by FA examination is more than 12 optic disc areas (1 optic disc area is 30.5mm2, a lesion including a bleeding, scar and neo-vascularization) in subject eye. 2) Patient with a scar or fibrosis in the range more than 50% of all lesions in subject eye. 3) Patients with a history of retinal pigment epithelium tear or rupture in subject eye. 4) Patients with a history of more than stage 3 macular hole in subject eye. 5) Patients with treatment of triamcinolone intravitreal injection within 6 months in subject eye. 6) Patient with a history of intraocular surgical operation (including cataract) within 3 months in subject eye. 7) Patient with a history of surgical operation such as vitrectomy and submacular surgery in subject eye. 8) Patients with intraocular, extraocular and periocular inflammation or infectious in either eye. 9) Patients with a history of uveitis in either eye. 10) Patients with serious allergic history to such as fluoresceine, indocyanine green, iodo. 11) Women who have pregnancy, possibility of the pregnancy or are nursing. 12) Any other patients who are regarded as unsuitable for this study by the investigators

研究者

发起方
Clinical Research Support Center Kyushu

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