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临床试验/EUCTR2006-005407-33-GB
EUCTR2006-005407-33-GB进行中(未招募)1 期

The effect of long-term iron treatment on serum NTBI and plasma isoprostanes in anaemic women versus an anaemic control group - NTBI and isoprostanes after long-term iron treatment

King's College London0 个研究点目标入组 30 人开始时间: 2006年10月16日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • •For the purposes of this study, we intend to recruit women of child-bearing age (18-50 years) only, as this sector of the population is the primary target group for supplemental iron. Only women age 18 - 50 with iron deficiency anaemia (haemoglobin < 12g/dl, mean cell volume < 90fl and serum ferritin < 20ug/l) will be included in this study.
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1.2 Adults (18-64 years) yes
  • •F.1.2.1 Number of subjects for this age range
  • •F.1.3 Elderly (>=65 years) no
  • •F.1.3.1 Number of subjects for this age range

排除标准

  • •Individuals will be excluded from partaking in this study if they:
  • •- suffer from serious chronic illness - have a body mass index above 30 - are a smoker - are taking prescription drugs including contraceptive medicines - regularly take medicines containing aspirin or ibuprofen - are pregnant or breastfeeding - are planning to become pregnant in the next 2 months
  • •- or have moderately/severely elevated cholesterol (>6.0 mmol/l), as these factors affect either iron absorption or plasma isoprostane concentration.

研究者

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