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Clinical Trial Summary

H. pylori positive patient volunteers that passed the selection criteria are recruited and divided into a test and a control group. Both groups are treated with a current treatment regime (EAC: Esomeprazole 40 mg/day; Clarithromycin 1000 mg/day; Amoxicillin 2000 mg/day) but only the test group received IgY-containing food supplement as an adjunctive measure for 15 days. The subjects are examined before and 4 weeks after the treatment initiation by Urea Breath Test (UBT) and gastro-endoscopy.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT02721355
Study type Interventional
Source Immunology Research Institute in Gifu
Contact
Status Completed
Phase N/A
Start date June 2013
Completion date June 2016