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Iron DeficiencyPhase 3HEIDCNCT00364104

Helicobacter Pylori Eradication Trial to Reduce Iron Deficiency in Children

A Phase 3 study testing Quadruple sequential Helicobacter pylori eradication + iron sulfate, Quadruple sequential Helicobacter pylori eradication therapy and Ferrous sulfate in people with Iron Deficiency, run by The University of Texas Health Science Center, Houston at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 36 to 120 monthsHealthy volunteers can take part
Conditions the study is for
Iron Deficiency
What is being tested?
Quadruple sequential Helicobacter pylori eradication + iron sulfate, Quadruple sequential Helicobacter pylori eradication therapy and Ferrous sulfate
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
125 participants
Where
1 siteUnited States
Study dates
Mar 2007to Dec 2008
Phase
Phase 3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 36 to 120 months
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

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

Who cannot join

  • 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
Show all 9Show fewer
  • 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

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Texas Tech University School of Medicine

    El Paso, Texas, 79905

Other trials in United States

About this study

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

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.

Read the 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:

  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.

Conditions
Iron Deficiency
Being tested
Quadruple sequential Helicobacter pylori eradication + iron sulfate, Quadruple sequential Helicobacter pylori eradication therapy, Ferrous sulfate, Placebo
Keywords
Iron deficiency, Helicobacter infection, Epidemiology
Medical subject headings
Iron Deficiencies, Helicobacter Infections

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Quadruple sequential Helicobacter pylori eradication + iron sulfateDrug

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

  • Quadruple sequential Helicobacter pylori eradication therapyDrug

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

  • Ferrous sulfateDrug

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

  • PlaceboDrug

    Placebo only (10-days of matching placebo of Hp eradication therapy and 6-weeks of matching iron supplementation).

Study groups in NCT00364104
Study groupRoleWhat they receive
AExperimentalA 10-day course of Hp infection sequential eradication therapy plus 6-weeks of iron supplementation
Receives: Drug: Quadruple sequential Helicobacter pylori eradication + iron sulfate
BExperimentalThe 10-day course of Hp infection sequential eradication therapy only plus 6-weeks of matching placebo of iron supplementation
Receives: Drug: Quadruple sequential Helicobacter pylori eradication therapy
CExperimental6-weeks of iron supplementation only plus 10-days of matching placebo of Hp infection eradication therapy
Receives: Drug: Ferrous sulfate
DPlacebo comparatorNot described
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Percent change of serum ferritin

    Measured: between 6 and 12 months

  2. Percent change of transferrin saturation

    Measured: between 6 and 12 months

  3. Percent change of hemoglobin

    Measured: between 6 and 12 months

Secondary outcomes (1)
  1. Proportion of children who cleared their H. pylori infection

    Measured: 45+ days after completing treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Aug 2006 (estimated)
  2. Study startMar 2007
  3. Primary completionDec 2008
  4. Study completionDec 2008

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Factorial
Masking
Triple blind
Who is masked
Participant, Care provider, Investigator
Enrolment
125 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00364104
Sponsor's protocol ID
HSC-SPH-06-0374
Acronym
HEIDC
Status last verified
Jun 2009
First submitted
14 Aug 2006
Last updated
30 Jun 2009
Results posted
No
Data monitoring committee
Yes

Publications

  • 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.

    PubMed 21336159
  • 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.

    PubMed 21336156

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Quadruple sequential Helicobacter pylori eradication + iron sulfate, Quadruple sequential Helicobacter pylori eradication therapy and Ferrous sulfate in people with Iron Deficiency, run by The University of Texas Health Science Center, Houston at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 30 Jun 2009. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Percent change of serum ferritin (time frame: between 6 and 12 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00364104, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Jun 2009.

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