Clinical Trials Directory

Trials / Completed

CompletedNCT05646784

Gut Microbiota in Mood Disorders in Lebanese Population

Pathophysiological Aspects of the Role of Inflammation and Gut Microbiota in Mood Disorders, and Their Therapeutic Implications in Lebanese Population

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
73 (actual)
Sponsor
St Joseph University, Beirut, Lebanon · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study aims to evaluate the pathophysiological aspects of the role of inflammation and gut microbiota in mood disorders, in particular in depression, and their therapeutic implications on a cohort of the Lebanese population. Specific objective: The evaluation of probiotic intake (CEREBIOME®, Lallemand Health Solutions Inc., Mirabel, Canada) on the inflammatory state, gut bacterial profile and the depressive state. Evaluate the effect of oral intake of a probiotic agent on plasma inflammatory markers, gut bacterial profile and depressive state in a subgroup of target patients versus a subgroup treated with placebo, in combination with conventional treatment.

Conditions

Interventions

TypeNameDescription
DRUGCerebiomeEvaluate the effect of oral intake of a probiotic agent on plasma inflammatory markers, gut bacterial profile and depressive state in a subgroup of target patients versus a subgroup treated with placebo
DRUGPlaceboPlacebo effect: Evaluate the effect of oral intake of a placebo, on clinical and plasma inflammatory markers, in a subgroup treated with placebo, in combination with conventional treatment for 12 weeks

Timeline

Start date
2024-01-24
Primary completion
2025-01-31
Completion
2025-01-31
First posted
2022-12-12
Last updated
2025-05-13

Locations

1 site across 1 country: Lebanon

Source: ClinicalTrials.gov record NCT05646784. Inclusion in this directory is not an endorsement.