A08 A09
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Male and female patients at the age of =18 - Patients with gastroenteritis - Written consent of the patient after information has been provided
Exclusion criteria
Exclusion criteria: - Patients who do not have diarrheal gastroenteritis (defined as 3 or more loose or liquid stools per day) - diseases that do not allow the person concerned to assess the nature and extent of the clinical trial and its possible consequences - Indications that the patient is unlikely to comply with the protocol (e.g., lack of cooperation)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Identification of "key"-bacteria and "key"-proteins associated with Norovirus-induced gastroenteritis | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Analysis of the dynamics within the intestinal microbiome and proteome in the natural course of norovirus-associated gastroenteritis with special focus on the identification of potential biomarkers 2. analysis of the composition of the proteome of intestinal exosomes with regard to specific patterns associated with norovirus-associated gastroenteritis 3. analysis of the composition of the intestinal microbiome for specific patterns associated with norovirus-associated gastroenteritis. 4. to determine the correlations between clinical, external and lifestyle factors with the risk of norovirus-associated gastroenteritis 5. to determine the correlations between clinical, external and lifestyle factors with the course of norovirus-associated gastroenteritis 6. analysis of FUT2 genotype and correlation with norovirus-associated gastroenteritis | — |
Countries
Germany
Contacts
Klinik für Gastroenterologie, Hepatologie und Endokrinologie, Medizinische Hochschule Hannover