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临床试验/NCT01519830
NCT01519830已完成4 期

Significance of Iron Deficiency in Transfusion Medicine: Effects of Iron Substitution on Fatigue Und General Well Being in Healthy Blood Donors

Insel Gruppe AG, University Hospital Bern1 个研究点 分布在 1 个国家目标入组 405 人开始时间: 2012年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
405
试验地点
1
主要终点
Difference of fatigue on a 10 point numeric scale after intravenous substitution of iron or placebo

研究概览

简要总结

Depletion of iron stores is frequently observed in regular blood donors, but effects of iron deficiency on general health is not well studied. Recent studies in women suffering of fatigue suggest iron deficiency without concomitant anemia as a common cause of these complaints. Provided the same is true in healthy subjects, substitution of intravenous iron might result in an improvement of general well being in iron depleted blood donors.

Healthy regular blood donors will be screened for low storage iron. Qualifying subjects will be invited to participate in a randomized, placebo-controlled trial with substitution of intravenous iron or placebo (saline solution). Differences in subjectively felt fatigue and other factors of general health and well being will be assessed. If an improvement of such factors can be shown after iron replacement, relevant concerns about artificially lowering iron stores by repeated phlebotomies will arise and changes of monitoring and substitution policies in blood banking might have to be discussed.

详细描述

Background

Chronic iron deficiency causes anemia with impairment of physical and mental capacity. Since iron plays an essential role in many enzymes apart from oxygen carriage, iron deficiency was proposed as an independent factor impairing wellbeing also without anemia. Symptoms like fatigue, asthenia, physical weakness, mental impairment and many others have been associated with iron deficiency. Recent clinical trials with iron substitution in iron deficient women suffering of general fatigue support this hypothesis, but data are still conflicting and debated.

Low body iron stores are frequently observed in blood donors. Repeated phlebotomies may induce or aggravate severe iron deficiency. Astonishingly, little is known about the long term effects of reduced iron stores on general health of regular blood donors. Serious health impairment cannot be excluded conclusively. Since many symptoms associated with iron deficiency are subtle, they might be missed by otherwise healthy subjects.

Blood donors with borderline or decreased iron stores (i.e. serum ferritin below 50 microg/l) will be invited to participate in a randomized, placebo-controlled intervention study comparing intravenous iron carboxymaltose and a physiological saline solution (placebo). Subjectively felt fatigue, measured on a numeric rating scale from 1 to 10 as the major end point will be assessed before and six months after application of the study drug. As additional factors, various aspects of general wellbeing will be assessed using four psychometric questionnaires. Statistical analysis will compare the results before and after application of the study drug and the results of the two study arms.

Objective

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Serum-Ferritin 50 microg/l
  • Eligibility for blood donation
  • At least one prior blood donation
  • Exclusion Criteria
  • Known intolerability of intravenous iron
  • History of anaphylactic reactions
  • Active systemic infections
  • Signs of chronic bleeding
  • Known iron overload
  • Lactation
  • Pregnancy
  • Any disease associated with increased fatigue
  • Medication associated with increased fatigue

排除标准

  • 未提供

研究组 & 干预措施

Verum

Experimental

Iron Carboxymaltose (Ferinject)

干预措施: Iron carboxymaltose (Ferinject) (Drug)

Placebo

Placebo Comparator

0.9% NaCl solution

干预措施: Placebo (Drug)

结局指标

主要结局

Difference of fatigue on a 10 point numeric scale after intravenous substitution of iron or placebo

时间窗: 6 weeks

measured by questionnaire

次要结局

  • Number of patients with adverse events of different grades(6 weeks)
  • Change of fatigue after intravenous substitution of iron(6 weeks)
  • Improvement of general wellbeing(6 weeks)

研究者

申办方类型
Other

研究点 (1)

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