Overview

Effect of Probiotics on Eradication of Persistent H.Pylori Infection

Status:
Not yet recruiting
Trial end date:
2023-09-10
Target enrollment:
0
Participant gender:
All
Summary
This study aims to investigate the possible safety and efficacy of probiotics (Bifidobacterium Infants, Enterococcus Feacium, and Lactobacillus Acidophilus) on the eradication rate of Helicobacter pylori and the incidence of adverse effects (AEs) of the concurrent rescue regimen in a patient with persistent H. Pylori infection.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Tanta University
Criteria
Inclusion Criteria:

- Symptomatic patients with persistent H. pylori infection of both sexes aged ≥ 18 years
old years whose infection was previously confirmed by endoscopy and pathology and
experienced ≥ 2 previous treatment failures.

Exclusion Criteria:

- Patients with penicillin allergy.

- Patients who have severe renal or hepatic disease.

- Patients who have severe cardiovascular, endocrinological or pulmonary disease.

- Patients with neoplastic diseases in the 5 years previous to recruitment.

- Patients with neurological or psychiatric pathology.

- Pregnant and/or lactating females

- Patients with a history of allergic reactions to any medications used in the
study.

- Patients with a history of taking proton pump inhibitors, H2 antagonists,
bismuth, or antibiotics (amoxicillin, metronidazole, clarithromycin) in the
previous 2 weeks.

- Patients on N-acetylcysteine

- Patients on drug or alcohol abuse in the past year.