EUCTR2005-002466-11-GB进行中（未招募）不适用
A Pilot Study to Examine the Safety and Efficacy of Posterior Juxtascleral Triamcinolone acetonide administration, in addition to Visudyne photoynamic therapy for predominantly Classic Choroidal Neovascularisation secondary to age related Macular degeneration: an open label randomised active controlled trial. - Efficacy of Juxtascleral Triamcinolone acetonide as an adjunct to PDT
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 80
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 age 50 years or above with a clinical diagnosis of wet AMD,confirmed to be predominantly classic on fluorescein angiography.
- •Visual acuity must be 6/60 or better.
- •Able to give informed consent.
- •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
- •Medical conditions that are likely to interfere with scheduled study visits.
- •Other ophthalmic conditions that may interfere with the assessment of treatment.
- •High degree of short sightedness.
- •Previous photodynamic therapy or other treatment for CNV,such as argon laser.
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