Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT05121025

Pathogen-microbiome Interaction During Helicobacter Pylori Infection

Led by University Hospital Freiburg · Updated on 2024-12-05

180

Participants Needed

1

Research Sites

198 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Pathogen-microbiome Interaction During Helicobacter Pylori Infection

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male and female patients aged 65 18 years
  • Specimens from patients undergoing tissue sampling, stool, and blood to rule out Helicobacter pylori infection
  • Written informed consent from patients
  • 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
Not Eligible

You will not qualify if you...

  • 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
  • Subjects not capable of giving consent
  • Subjects with acute illnesses
  • Subjects older than 65 or younger than 18 years of age
  • Pregnant women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Institute for Microbiology and Hygiene

Freiburg im Breisgau, Baden-Wurttemberg, Germany, 79104

Actively Recruiting

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Research Team

M

Mohamed Tarek Badr, M.D.

CONTACT

A

Anne Lichtenegger

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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