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Impact of sauerkraut consumption on metabolic control, inflammatory status and host-microbiome-interactions - Trial DRKS00027007

Access comprehensive clinical trial information for DRKS00027007 through Pure Global AI's free database. This phase not specified trial is sponsored by Universitätsklinikum FreiburgProf. Dr. Dr. Karin MichelsElsässer Straße 279110 FreiburgGermany and is currently Recruitment Completed. The study focuses on None ;Healthy volunteers.

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DRKS00027007
Recruitment Completed
Trial Details
Deutsches Register Klinischer StudienDRKS00027007
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Impact of sauerkraut consumption on metabolic control, inflammatory status and host-microbiome-interactions

Study Focus

None ;Healthy volunteers

Interventional

Sponsor & Location

Universitätsklinikum FreiburgProf. Dr. Dr. Karin MichelsElsässer Straße 279110 FreiburgGermany

Universitätklinikum Freiburg Institut für Prävention und TumorepidemiologieElsässer Straße 279110 FreiburgGermany

Germany

Timeline & Enrollment

N/A

N/A

N/A

Summary

The gut microbiome has been associated with a number of diseases including obesity and holds great potential for the treatment or prevention of various illnesses. Fresh fermented vegetables, such as sauerkraut, contain a large number of lactic acid bacteria that may have beneficial effects on host metabolism. We therefore hypothesize that daily consumption of sauerkraut with live lactic acid bacteria improves metabolic and inflammatory status of healthy and overweight study participants via modulation of the gut microbiome. Furthermore, we expect a similar effect from consumption of pasteurized sauerkraut with heat-killed bacteria compliant with the postbiotic concept (a postbiotic is a “preparation of inanimate microorganisms and/or their components that confers a health benefit on the host”).

ICD-10 Classifications

Healthy person accompanying sick person
Routine general health check-up of armed forces
Routine general health check-up of sports teams
Routine general health check-up of inhabitants of institutions

Data Source

Deutsches Register Klinischer Studien

DRKS00027007

Non-Device Trial