Helicobacter Pylori Eradication Trial to Reduce Iron Deficiency in Children (HEIDC)
Iron Deficiency
About this trial
This is an interventional prevention trial for Iron Deficiency focused on measuring Iron deficiency, Helicobacter infection, Epidemiology
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
Sites / Locations
- Texas Tech University School of Medicine
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Experimental
Experimental
Placebo Comparator
A
B
C
D
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