CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 73 enrolled
Drug / intervention
Cerebiome +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05646784
NCT05646784N/ACompleted

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

St Joseph University, Beirut, Lebanon·interventional·Posted Dec 12, 2022·Updated May 13, 2025

In Brief

A clinical study evaluating Cerebiome and Placebo for Gut Microbiome and Mood Disorders. Completed, enrolled 73 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesLebanon

Timeline

N/ACompletedFinished
2023202420252026
First PostedDec 12, 2022
Enrollment StartJan 24, 2024
Primary CompletionJan 31, 2025
TodayJul 2, 2026
Enrollment to primary: 1.0 yearsPosted 3.6 years ago

Interventions

Cerebiomedrug

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

Placebodrug

Placebo 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