跳至主要内容
临床试验/NCT00210002
NCT00210002终止2 期

Evaluation of Systematic Intravenous Iron Supplementation During Darbepoetin Alfa Treatment in Prophylaxis of Severe Anaemia Chemo-Induced.

Institut Claudius Regaud4 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2003年11月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
55
试验地点
4
主要终点
Biological response rate for each group.

研究概览

简要总结

The purpose of this study is to evaluate the response rate obtained in an heterogeneous oncologic population treated by chemotherapy, and either by Darbepoetin alfa classic treatment or by association of Darbepoetin alfa -ferric saccharose systematic supplementation, administered concomitantly with chemotherapy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
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

  • Age ≥ 18 years
  • Well-informed written consent, signed by the patient
  • Patient picked up for solid tumor treatment, whichever the localization, with or without metastasis
  • Patient revealing, before or during chemotherapy, a moderate anemia, that means: Men: 9<Hb<12 g/dl; Women: 9<Hb<11 g/dl.
  • Patient for who at least four chemotherapy cycles are planed (eight in case of weekly chemotherapy) after inclusion in the study
  • Patients with life expectancy higher than three months
  • Patient with general conditions compatible with the study's follow-up

排除标准

  • Contra-indication for Venofer
  • Anemia which can have curative treatment
  • Bloody transfusion during the previous four weeks
  • Documented or suspected medullary invasion
  • Uncontrolled arterial hypertension
  • Acute bacterial infection
  • Transferrin saturation's coefficient
  • Pregnancy
  • Ferric salts oral treatment interrupted since less than one week
  • Patient with bad french language's comprehension
  • Patient with a major psychiatric pathology
  • Patient under guardianship, trusteeship or justice safeguard

结局指标

主要结局

Biological response rate for each group.

次要结局

  • To determine tolerance for ferric saccharose (Venofer®)
  • To determine percentage of patients who necessitate an increase of Darbepoetin alfa's dose(Aranesp®)
  • To determine percentage of hemoglobin rate's correction
  • To determine biological parameters's evolution

研究者

申办方类型
Other

研究点 (4)

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