EUCTR2009-014280-38-GB进行中(未招募)1 期
A randomised controlled trial of standard and low dose Avastin® for Neovascular Macular Degeneration in the East Midlands - TANDEM: RCT of standard & low dose Avastin for MD in East Midlands
ottingham University Hospitals NHS Trust0 个研究点目标入组 812 人开始时间: 2010年8月3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
- 812
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
入选标准
- •Any patient newly referred for the treatment of nAMD or reactivation of nAMD, i.e. disease stable with no treatment for nAMD to either eye for the previous 6 months, who is considered eligible for anti-VEGF treatment in the NHS.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 600
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 1400
排除标准
- •Pregnant and or lactating women • Women with child bearing potential (i.e. not sterilised or not post menopausal) who are unwilling to use contraception • Men with a spouse or partner with child bearing potential unless the participant has agreed to use condoms • Patients with known hypersensitivity to recombinant human or humanised antibodies
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