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临床试验/NCT00331435
NCT00331435已完成4 期

Clinical Research of Photodynamic Therapy for Exudative Age-related Macular Degeneration Accompanied With Polypoidal Choroidal Vasculopathy

Ophthalmic PDT Study Group27 个研究点 分布在 1 个国家目标入组 113 人开始时间: 2006年6月1日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
113
试验地点
27
主要终点
Proportion of study eyes which best corrected visual acuity (BCVA) improves 2 lines or more or maintains (+/-1 line changes) at 12 months after first treatment, as compared with the visual acuity at baseline period.

研究概览

简要总结

The purpose of this study is to evaluate and conduct an exploratory comparison of the efficacy and safety of indocyanine green angiography (ICGA) guided photodynamic therapy (PDT) and fluorescein angiography (FA) guided PDT for exudative age-related macular degeneration (AMD) accompanied with polypoidal choroidal vasculopathy (PCV).

详细描述

PDT with verteporfin has been proven beneficial for patients with AMD. The laser spot size is decided based on FA finding (FA guided PDT). ICGA is needed to detect PCV lesions, such as polypoidal lesions or abnormal network vessels. In clinical practice, PDT based on ICGA (ICGA guided PDT) has and is being conducted for the treatment of AMD with PCV. However, there are no reports on the outcomes of prospective research of PDT for PCV in Japanese patients. Furthermore, there are no reports comparing FA guided PDT and ICGA guided PDT.

We propose to conduct this clinical research in order to investigate the efficacy and safety of PDT for PCV in Japanese patients, and to compare results of FA guided PDT and ICGA guided PDT.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Japanese patients aged 50 years old or older
  • Exudative AMD with subfoveal PCV
  • Eyes with PCV meets the definite criteria of PCV issued from Japanese study group of Polypoidal Choroidal Vasculopathy
  • PCV lesion with subfoveal hemorrhage or exudation
  • Lesion size (GLD) of less than 12 MPS Disc area measured by FA and IA.
  • Decimal BCVA of 0.1-0.5 at baseline period.

排除标准

  • Patients who have RPE tear, vitelliform retinal dystrophy, and central Serous Chorioretinopathy.
  • Patients who have other ocular disease with irreversible VA
  • Study eyes unable to be taken fundus photos of CNV
  • Study eyes received surgery operation within 2 months of the participation to this study or ND:YAG operation within one month
  • Pathological myopia
  • PCV with cleary identified subsensory retinal CNV (on the RPE) at the baseline examination
  • Study eyes which have received any treatments for CNV, such as PDT, transpupillary thermotherapy, laser photocoagulation, and so on.
  • Patients who have any physical problem for using angiography or PDT (such as systemic debility, significant diabetes mellitus, significant heart disease, and so on)
  • Medical history of porphyria, porphyrin sensitivity, or hypersensitivity to sunlight or bright light.
  • Patients with medical history of hypersensitivity to ingredients of Visudyne
  • Patients with medical history of hypersensitivity to ingredients of fluorescein or indocyanine green injection
  • Patients with hypersensitivity to iodine
  • Patients judged inappropriate for this study by the investigator

结局指标

主要结局

Proportion of study eyes which best corrected visual acuity (BCVA) improves 2 lines or more or maintains (+/-1 line changes) at 12 months after first treatment, as compared with the visual acuity at baseline period.

时间窗: 12 months

次要结局

  • PCV lesion size based on ICGA.(0-12 month)
  • Mean number of PDT treatments required during the study period.(12 month)
  • Proportion of number of study eyes which BCVA improves 3 lines or more or maintains (+/-1 line), as compared with baseline examination.(12 month)
  • Change of findings of polypoidal lesions.(0-12 month)
  • Choroidal neovascularization (CNV) closure based on FA.(0-12 month)
  • Factor affecting to change in visual acuity.(12month)
  • Change of findings of abnormal network vessels.(0-12 month)
  • Change in subretinal fluid at the fovea and central retinal thickness based on optical coherence tomography (OCT).(0-12month)
  • Proportion of eyes with decimal BCVA of 0.5 or more.(12 month)
  • Change in greatest linear dimension (GLD) based on FA.(0-12 month)

研究者

发起方
Ophthalmic PDT Study Group
申办方类型
Other

研究点 (27)

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