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临床试验/NCT00430547
NCT00430547已完成不适用

Thyroid-Associated Ophthalmopathy Subtypes and Orbital Antibodies

Barwon Health2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2003年8月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Barwon Health
入组人数
60
试验地点
2
主要终点
Onset or progression of ophthalmopathy following radio-active iodine therapy

研究概览

简要总结

The purpose of this study is to determine whether radioactive iodine, as compared to anti-thyroid medications, is a risk factor for the development or progression of thyroid-associated ophthalmopathy in patients with hyperthyroidism due to Graves' disease. The other aim of this study is to determine the incidence of the various ophthalmopathy subtypes and the utility of orbital antibodies in the diagnosis, classification and monitoring of patients with thyroid-associated ophthalmopathy.

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
None

入排标准

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

入选标准

  • Graves' disease diagnosed in the last 3 months, regardless of the presence of ophthalmopathy

排除标准

  • Pre-existing eye disease: e.g. orbital surgery, orbital irradiation or significant loss of vision
  • Age < 18 years
  • Inability to consent to participation in the study
  • Pregnancy
  • History of radio-active iodine therapy

结局指标

主要结局

Onset or progression of ophthalmopathy following radio-active iodine therapy

次要结局

未报告次要终点

研究者

发起方
Barwon Health
申办方类型
Other Gov

研究点 (2)

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