ISRCTN33957677已完成不适用
A pilot study to examine the safety and efficacy of posterior juxta-scleral (80 mg) triamcinolone acetonide, administration, in addition to Visudyne (verteporfin) photodynamic therapy for predominantly classic choroidal neovascularisation secondary to age-related macular degeneration: an open-label, randomised, active controlled trial
King's College Hospital (UK)0 个研究点目标入组 80 人开始时间: 2008年1月18日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 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
入排标准
- 性别
- All
入选标准
- •1. Age 50 years or older, male and female
- •2. Clinical diagnosis of age-related macular degeneration (AMD)
- •3. Subfoveal choroidal neovascularisation (CNV) confirmed by fluorescein angiography
- •4. Best corrected visual acuity of 35 letters on Early Treatment Diabetic Retinopathy Study (ETDRS) chart
排除标准
- •1. Inability to understand or sign consent form
- •2. The patient has a current medical condition or history of a medical condition that would be likely to preclude scheduled study visits
- •3. Patient has a current ophthalmic condition or history of an ophthalmic condition that might compromise the assessment of the treatment
- •4. Signs of a myopic retina or refraction of greater than -8 dioptres in their current or previous glasses prescription
- •5. Signs of other retinal conditions that may have caused the CNV such as angioid streaks, choroidal rupture, and old chorio-retinitis
- •6. Open angle glaucoma
- •7. At increased risk of developing glaucoma such as having; pigment dispersion syndrome or pseudoexfoliation
- •8. Unable to have a good quality fluorescein angiogram taken, e.g., due to head tremor or media opacity
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