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临床试验/NCT01376622
NCT01376622已完成不适用

Changes in Pituitary Iron and Volume With Deferasirox in Transfusional Iron Overload

Children's Hospital Los Angeles1 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2008年11月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
130
试验地点
1

研究概览

简要总结

Despite continuing advances in iron chelation therapy, iron toxicity of endocrine glands, particularly the pituitary gland, remains common in patients with transfusion dependent anemias. We would like to establish accurate population norms of pituitary R2 and volume and understand the progression of pituitary iron in transfused patients on Deferasirox.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
2 Years 至 25 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Currently on chronic transfusion therapy.
  • Duration of chronic transfusion >1 year.
  • Age 2 to 25 years
  • On deferasirox monotherapy for the duration of the study.
  • Informed consent from legal guardian and/or patient.
  • On deferasirox for a minimum of 3 months at start of study.

排除标准

  • Sickle cell disease or sickle-beta zero genotype.
  • Combination of deferasirox and another iron chelator.

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

John C. Wood

Principal Investigator

Children's Hospital Los Angeles

研究点 (1)

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