CTRI/2010/091/000379招募中4 期
A study to evaluate the effect of Lucentis® (Ranibizumab) on Vision Related Function using the VFQ-25 questionnaire in patients with wet age-related macular degeneration (AMD)
ovartis health care private limited0 个研究点目标入组 500 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 500
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
入选标准
- •1.Diagnosed with choroidal neovascularization (CNV) secondary to (wet) AMD
- •2.Willing to provide informed consent (as per the local practices)
- •Patients may have received Lucentis monotherapy or combination therapy [with Visudyne® (verteporfin)]
排除标准
- •1.Hypersensitivity to the active substance or to any of the excipients.
- •2.Patients with active or suspected ocular or periocular infections.
- •3.Patients with active intraocular inflammation.
研究者
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