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Clinical Trials in Sweden / NCT07046897
Recruiting Not applicable

Analysis of the Gut Microbiota Composition After Consumption of Probiotic Bacteria

NCT07046897 · tracked via the Priya Life Science Sweden tracker
Phase
Not applicable
Started
2024-11-12
Last updated
2025-07-02

Condition(s) studied

Microbiota Analysis in Healthy Subjects

Investigational drug(s) / intervention(s)

Consumption of probiotics strain 5Consumption of probiotics strain 6

Consumption of probiotics strain 5: Consumption of probiotic capsules containing the probiotic bacteria Bacillus coagulans strain 5.

Consumption of probiotics strain 6: Consumption of probiotic capsules containing the probiotic bacteria Bacillus coagulans strain 6.

Study summary

The goal of this intervention study is to evaluate the beneficial effect of the probiotic bacterium Bacillus coagulans in healthy volunteers. The main question it aims to answer is if the probiotic strains are modifying the microbiota composition in a beneficial way, evaluated in faecal- and saliva samples.

Primary hypothesis: The probiotic bacteria will modify the microbiota composition in faecal- and saliva samples.

Participants will consume the freeze-dried probiotic bacteria for 14 days. Before and after consumption, the participants will collect samples.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: • You must be 18-65 years of age. Exclusion Criteria: * Participants must not be diagnosed with gastrointestinal diseases, autoimmune diseases or have diseases or medications that cause immune deficiency such as MS, type 1 diabetes, cancer or HIV. * Participants must not have taken antibiotics in the month before or during the study. * Participants must not consume other probiotic products or fermented foods during the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Process and Life Science Engineering, Lund University Lund Sweden Recruiting

More Lund University trials in Sweden

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07046897 on ClinicalTrials.gov ↗ ← All trials in Sweden