Phase
Condition
Stress
Treatment
Pasteurized Akkermansia muciniphila
Placebo
Clinical Study ID
Ages 18-70 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Working in a high stress hospital department, like: emergency, trauma, intensivecare, surgery, internal diseases;
Written informed consent to participate in this study before any study-mandatedprocedure;
Body mass index (BMI) ≥18.5 kg/m2 and ≤ 35 kg/m2;
A willingness and motivation to follow the study protocol.
Exclusion
Exclusion Criteria:
Diagnosis of autoimmune, neurological, immunocompromised, thyroid, inflammatorybowel diseases, irritable bowel syndrome, diabetes, cancer, and/or IgE-dependentallergy;
Psychiatric comorbidities, including mental retardation, organic brain dysfunction,or addiction (except nicotine and caffeine), intake of antipsychotic andantidepressive drugs;
Proton pump inhibitors usage;
The use of antibiotics and/or probiotics 4 weeks prior to the study;
Glucocorticosteroids and/or metformin treatment;
Dietary supplementation (except for vitamin D) within the three months beforescreening;
Specific restrictive (e.g. elimination, vegan, FODMAP, reduction) diet within thethree months before screening;
Significant changes in physical activity 4 weeks before the trial entry;
Pregnancy or lactation;
Significant GI surgery within the last 6 months prior to or planned during thestudy;
Any other medication for management of IBS complaints like peppermint oil, bile acidbinders;
Lactose intolerance;
Participation in another study during the last 30 days prior to and during thestudy;
Any other reason for exclusion as per investigator's judgment, e.g. insufficientcompliance with study procedures.
Study Design
Study Description
Connect with a study center
Center fo Medical Simulation
Szczecin, Zachodniopomorskie 71-240
PolandSite Not Available
Pomeranian Medical University in Szczecin
Szczecin, Zachodniopomorskie 70-210
PolandSite Not Available

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