跳至主要内容
临床试验/NCT00308490
NCT00308490已完成4 期

Phase IV Study of Iron Indices' Kinetics in Hemodialysis Patients

Papageorgiou General Hospital2 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2005年9月1日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
160
试验地点
2
主要终点
Ferritin alterations after iron loading at six and twelve weeks from the beginning of iron loading.

研究概览

简要总结

The purpose of this study is to describe alterations of serum ferritin, transferrin saturation, soluble transferrin receptor, % hypochromic erythrocytes, % reticulocytes, reticulocyte hemoglobin content after iron loading in hemodialysis patients.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Diagnostic
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

  • hemodialysis for three months minimum
  • stable epoetin dose for two months minimum
  • serum ferritin concentration < 1000 ng/ml
  • transferrin saturation < 50%
  • parathormone concentration < 800 pg/ml

排除标准

  • hemoglobin concentration > 13g/dl
  • serum ferritin concentration < 20 ng/ml
  • vitamin B12 and/or folic deficiency
  • other hematologic disease than anemia
  • hypothyroidism
  • infectious disease

结局指标

主要结局

Ferritin alterations after iron loading at six and twelve weeks from the beginning of iron loading.

次要结局

  • All iron indices' alterations during twelve weeks from the beginning of iron loading.

研究者

发起方
Papageorgiou General Hospital
申办方类型
Other

研究点 (2)

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