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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05121025
Other study ID # 21/1552
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 11, 2022
Est. completion date June 1, 2025

Study information

Verified date November 2023
Source University Hospital Freiburg
Contact Mohamed Tarek Badr, M.D.
Phone 00497612036585
Email mohamed.tarek.badr@uniklinik-freiburg.de
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Helicobacter pylori affects the gut microbiome in ways that are only partially understood. In which patients H. pylori causes severe disease and in whom it merely colonizes, possibly even with beneficial effects, is not understood. The investigators are pursuing the hypothesis that changes in the gut microbiome that can be easily measured in stool have such predictive value.


Description:

Helicobacter pylori colonizes the stomach of about half of the world's population, including about 20-30% of adults in Germany. In some cases, this colonization can lead to chronic inflammation of the gastric mucosa, which can lead to various serious diseases such as ulcer disease and gastric cancer. It has been reported several times in the literature that Helicobacter pylori infection negatively affects the human intestinal flora and can lead to microbial imbalance (dysbiosis). Recent studies, mostly from mouse models, reveal new roles and interactions of the microbiome: host immune response may influence bacterial activity; bacterial metabolites may determine microbiome functions. Differences in the microbiome were also found between Helicobacter pylori-infected patients and were associated with treatment success. On the other hand, beneficial microbial symbiosis may prevent intestinal inflammation. The reasons for these differences in the microbiome of Helicobacter pylori-infected patients, which may also contribute to treatment failure, remain to be investigated. Therefore, this project aims to investigate how Helicobacter pylori affects the bacteria and fungi of the human gastrointestinal microbiome and how the suspected microbial imbalance may influence treatment success. In this project, The investigators aim to answer the question of how these newly discovered mechanisms alter the course of human H. pylori infection. The investigators will analyze H. pylori itself in colonized patients and asymptomatic individuals (whole genome sequencing), determine the immune response of the carrier (RNA expression in lymphocytes), and composition of the gut microbiome (DNA sequencing) and activity (RNA expression in the bacteria/fungi and identification of metabolites). Using bioinformatics approaches, particularly machine learning, The investigators will determine the parameters that predict disease progression and eradication success. The results will provide important decision support for H. pylori-infected patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 180
Est. completion date June 1, 2025
Est. primary completion date June 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: Patients: - - Male and female patients aged = 18 years. - Specimens from patients undergoing tissue sampling, stool, and blood to rule out Helicobacter pylori infection - Written informed consent from patients. Volunteer subjects: - - Male and female (non-pregnant) volunteers between the ages of 18-65 years. - Written informed consent from volunteers. - No acute medical conditions - No regular medication use, and no antibiotic use in the last 4 weeks. Exclusion Criteria: Patients: - - Minor patients - Patients not capable of giving consent - Samples without sufficient residual material after standard diagnostic procedures - Samples from patients who have not given consent for testing Volunteer subjects: - - Subjects not capable of giving consent - Subjects with acute illnesses - Subjects older than 65 or younger than 18 years of age. - Pregnant women

Study Design


Intervention

Diagnostic Test:
Analysis of gut microbiome and immune signatures
The investigators will analyse the microbiome composition (16S rDNA-sequencing and metagenomics), microbiome activity (RNA-sequencing of stool bacteria and metabolite sampling) and immune cell activity (leukocyte RNA-sequencing) of all study groups.

Locations

Country Name City State
Germany Institute for Microbiology and Hygiene Freiburg Baden Württemberg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Freiburg

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Helicobacter pylori microbiome and immune signatures The diversity of the gut microbial species of patients and controls as well as transcriptomic signatures of blood immune cells will be assessed and compared to conclude specisifc signatures that are associated with the disease and carrier status. These signatures will be analyzed to identify specific bacterial and immune biomarkers that can be used as a screening tool for Helicobacter pylori infection. 12-18 Months
Secondary Helicobacter pylori eradication control Patients with positive gastric biopsy for Helicobacter pylori will be assessed for successful eradication after treatment, and the eradication success will be compared with the patients' microbial signatures to identify specific gut microbial signatures that are associated with treatment outcome. 12-24 Months
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