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Helicobacter Pylori Eradication Trial to Reduce Iron Deficiency in Children (HEIDC)

Primary Purpose

Iron Deficiency

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Quadruple sequential Helicobacter pylori eradication + iron sulfate
Quadruple sequential Helicobacter pylori eradication therapy
Ferrous sulfate
Placebo
Sponsored by
The University of Texas Health Science Center, Houston
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Iron Deficiency focused on measuring Iron deficiency, Helicobacter infection, Epidemiology

Eligibility Criteria

36 Months - 120 Months (Child)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Texas Tech University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

A

B

C

D

Arm Description

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

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

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

Outcomes

Primary Outcome Measures

Percent change of serum ferritin
Percent change of transferrin saturation
Percent change of hemoglobin

Secondary Outcome Measures

Proportion of children who cleared their H. pylori infection

Full Information

First Posted
August 14, 2006
Last Updated
June 26, 2009
Sponsor
The University of Texas Health Science Center, Houston
Collaborators
Texas Tech University, University of Texas, Baylor College of Medicine, University of North Texas Health Science Center
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1. Study Identification

Unique Protocol Identification Number
NCT00364104
Brief Title
Helicobacter Pylori Eradication Trial to Reduce Iron Deficiency in Children
Acronym
HEIDC
Official Title
Randomized Field Intervention Trial of H. Pylori Eradication to Reduce Iron Deficiency Among Children in El Paso, Texas
Study Type
Interventional

2. Study Status

Record Verification Date
June 2009
Overall Recruitment Status
Completed
Study Start Date
March 2007 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
The University of Texas Health Science Center, Houston
Collaborators
Texas Tech University, University of Texas, Baylor College of Medicine, University of North Texas Health Science Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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: serum ferritin, transferrin saturation, and 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Iron Deficiency
Keywords
Iron deficiency, Helicobacter infection, Epidemiology

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
125 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
A 10-day course of Hp infection sequential eradication therapy plus 6-weeks of iron supplementation
Arm Title
B
Arm Type
Experimental
Arm Description
The 10-day course of Hp infection sequential eradication therapy only plus 6-weeks of matching placebo of iron supplementation
Arm Title
C
Arm Type
Experimental
Arm Description
6-weeks of iron supplementation only plus 10-days of matching placebo of Hp infection eradication therapy
Arm Title
D
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Quadruple sequential Helicobacter pylori eradication + iron sulfate
Intervention Description
A 10-day course of Hp infection sequential eradication therapy plus 6-weeks of iron supplementation
Intervention Type
Drug
Intervention Name(s)
Quadruple sequential Helicobacter pylori eradication therapy
Intervention Description
A 10-day course of Hp infection sequential eradication therapy only plus 6-weeks of matching placebo of iron supplementation
Intervention Type
Drug
Intervention Name(s)
Ferrous sulfate
Intervention Description
6-weeks of iron supplementation only plus 10-days matching placebo of Hp infection eradication therapy
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo only (10-days of matching placebo of Hp eradication therapy and 6-weeks of matching iron supplementation).
Primary Outcome Measure Information:
Title
Percent change of serum ferritin
Time Frame
between 6 and 12 months
Title
Percent change of transferrin saturation
Time Frame
between 6 and 12 months
Title
Percent change of hemoglobin
Time Frame
between 6 and 12 months
Secondary Outcome Measure Information:
Title
Proportion of children who cleared their H. pylori infection
Time Frame
45+ days after completing treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
36 Months
Maximum Age & Unit of Time
120 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Children 3-10 years of age Helicobacter pylori infected, asymptomatic Healthy otherwise Parents provided consent/assenting children 7-10 years of age Exclusion Criteria: 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Victor M Cardenas, MD, MPH, PhD
Organizational Affiliation
University of Texas-Houston School of Public Health El Paso Regional Campus
Official's Role
Principal Investigator
Facility Information:
Facility Name
Texas Tech University School of Medicine
City
El Paso
State/Province
Texas
ZIP/Postal Code
79905
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21336159
Citation
Cardenas VM, Prieto-Jimenez CA, Mulla ZD, Rivera JO, Dominguez DC, Graham DY, Ortiz M. Helicobacter pylori eradication and change in markers of iron stores among non-iron-deficient children in El Paso, Texas: an etiologic intervention study. J Pediatr Gastroenterol Nutr. 2011 Mar;52(3):326-32. doi: 10.1097/MPG.0b013e3182054123.
Results Reference
derived
PubMed Identifier
21336156
Citation
Prieto-Jimenez CA, Cardenas VM, Fischbach LA, Mulla ZD, Rivera JO, Dominguez DC, Graham DY, Ortiz M. Double-blind randomized trial of quadruple sequential Helicobacter pylori eradication therapy in asymptomatic infected children in El Paso, Texas. J Pediatr Gastroenterol Nutr. 2011 Mar;52(3):319-25. doi: 10.1097/MPG.0b013e318206870e.
Results Reference
derived

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Helicobacter Pylori Eradication Trial to Reduce Iron Deficiency in Children

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