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临床试验/NCT00364104
NCT00364104已完成3 期

Randomized Field Intervention Trial of H. Pylori Eradication to Reduce Iron Deficiency Among Children in El Paso, Texas

The University of Texas Health Science Center, Houston1 个研究点 分布在 1 个国家目标入组 125 人开始时间: 2007年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
125
试验地点
1
主要终点
Percent change of serum ferritin

研究概览

简要总结

The investigators hypothesize that the Helicobacter pylori bacterium decreases iron from the stomach and that this effect of the infection can be identified among persons with iron deficiency as well as among persons with normal iron stores. The aim of this study is to determine whether Helicobacter pylori eradication in children is followed by an increase in markers of iron stores after six to twelve months of treatment.

详细描述

For the last 12 years, scientific evidence has mounted linking Helicobacter pylori infection with iron deficiency and iron deficiency anemia. Reports from around the world on several cases of iron deficiency anemia refractory to iron supplementation among children infected with Helicobacter pylori, most without evident ulcers, clearly indicate that such cases have been cured of their anemia after receiving a course of Helicobacter pylori eradication therapy. Several studies based on national surveys, including one on the U.S. National Health and Nutrition Examination Survey data and conducted by the authors of this proposal, have found an association between Helicobacter pylori infection and the levels of iron stores. However, these studies fail to demonstrate that anemia follows Helicobacter pylori infection. Moreover, most previous research has been conducted outside of the contiguous U.S. and has not included young children, one of the high-risk populations for iron deficiency and iron deficiency anemia. Data on this age-group is most needed to develop sound public health interventions.

We propose to conduct such a study among children living in El Paso, Texas, a city located on the U.S.-Mexico border. A series of studies have been conducted in that city by the authors of this proposal, including a National Institutes of Health sponsored study aiming to describe the natural history of Helicobacter pylori infection in children from birth to age seven years (84 months). We hypothesize that the Helicobacter pylori bacterium decreases iron from the stomach and that this effect of the infection can be identified among persons with iron deficiency as well as among persons with normal iron stores. Currently, the clinical management of the most extreme form of iron deficiency, that is iron deficiency anemia, relies only on supplemental iron therapy. For ethical reasons, our study will identify children with anemia from the study, and will assign them to one of the arms receiving iron supplementation. Our study will determine whether a combination of iron supplementation and sequential Helicobacter pylori eradication therapy yields higher increases of iron stores than each of these treatments alone. To summarize, our main hypothesis is that Helicobacter pylori infection is associated with iron deficiency such that Helicobacter pylori eradication would result in an increase in the levels of:

  1. serum ferritin,
  2. transferrin saturation, and
  3. hemoglobin.

To test these hypotheses we will randomly assign 125 Helicobacter pylori-infected children (3 to 10 years of age) into each of the following four groups: Helicobacter pylori eradication treatment, iron supplementation, Helicobacter pylori eradication plus iron supplementation, or placebo. We plan to recruit infected children through a household survey in El Paso, screen their Helicobacter pylori infection status by a stool test, and invite their parents to undergo a confirmatory breath test. Infected children randomly allocated to those four arms of the study will be followed closely during the 6 weeks they are taking the study medication to record any adverse event, followed by a visit at 45 days after treatment to tell whether or not those receiving the medication had their infection eradicated, between 6 and 12 months for hematological evaluation to compare with the baseline levels of iron stores.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
36 Months 至 120 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Children 3-10 years of age
  • Helicobacter pylori infected, asymptomatic
  • Healthy otherwise
  • Parents provided consent/assenting children 7-10 years of age

排除标准

  • Parental consent or child assent not obtained
  • History of antibiotic-related allergic episodes
  • Children with a history of allergy, asthma, hay fever or urticaria
  • Phenylketonurics
  • Abnormal renal and hepatic functions as evaluated through albumin, bilirubin, AST (or SGOT), ALT (or SGPT), alkaline phosphatase and GGT-P
  • History of peptic ulcer
  • History of recent (< 1 month) severe disease
  • History of recent (< 1 month) use of antibiotics, antacids, H2 receptor antagonists, proton pump inhibitors and remedies containing bismuth
  • Parents uncertain about staying in El Paso for the next year

研究组 & 干预措施

A

Experimental

A 10-day course of Hp infection sequential eradication therapy plus 6-weeks of iron supplementation

干预措施: Quadruple sequential Helicobacter pylori eradication + iron sulfate (Drug)

B

Experimental

The 10-day course of Hp infection sequential eradication therapy only plus 6-weeks of matching placebo of iron supplementation

干预措施: Quadruple sequential Helicobacter pylori eradication therapy (Drug)

C

Experimental

6-weeks of iron supplementation only plus 10-days of matching placebo of Hp infection eradication therapy

干预措施: Ferrous sulfate (Drug)

D

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Percent change of serum ferritin

时间窗: between 6 and 12 months

Percent change of transferrin saturation

时间窗: between 6 and 12 months

Percent change of hemoglobin

时间窗: between 6 and 12 months

次要结局

  • Proportion of children who cleared their H. pylori infection(45+ days after completing treatment)

研究者

研究点 (1)

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