Effect of gastrointestinal infection eradication on iron stores

Not Applicable

• Conditions: Condition 1: Helicobacter Pylori Infection. Condition 2: Iron Deficiency.; Helicobacter pylori [H. pylori] as the cause of diseases classified elsewhere; Iron deficiency anemia, unspecified; B96.81

• Registration Number: IRCT2016021626593N1
• Lead Sponsor: Zahedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 108

Inclusion Criteria

patients with dyspepsia symptoms who their H pylori infection was proven by endoscopy and biopsy; ferritin serum level less than 40 ng /ml; negative CRP test.

Exclusion criteria: History of treatment of helicobacter pylori during last 6 months; history of iron supplement intake among last 6 months; known underlying diseases associated with iron deficiency; lack of informed consent.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hemoglubin. Timepoint: Before Intervention. Method of measurement: Sysmex K21.;CRP. Timepoint: Before Intervention. Method of measurement: Latex Aglutination.;Ferritin. Timepoint: Before and After Intervention. Method of measurement: Eliza Method.

Secondary Outcome Measures

Name	Time	Method
Ferritin. Timepoint: After Intervention. Method of measurement: Eliza Method.;Helicobacter Pylori Fecal Antigen. Timepoint: After Intervention. Method of measurement: Stool Examination.