Institut sur la nutrition et les aliments fonctionnels (INAF)
Québec, Quebec, G1V 0A6, Canada
Location status: Recruiting
NCT Number: NCT06704321
This clinical trial aims to investigate the effects of TOTUM-448, a mix of 5 plant extracts and choline, consumed at the daily regimen of two times per day, on liver fat content, cardiometabolic risk factors and gut microbiota among both men and women with MASLD.
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Not applicable
Québec, Quebec, G1V 0A6, Canada
Location status: Recruiting
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Main Inclusion Criteria:
Main Exclusion Criteria:
16 weeks of TOTUM-448 supplementation (4.284g/day corresponding to 8 capsules per day)
16 weeks of placebo supplementation (8 capsules per day)
Time frame: Baseline (V1) and End of supplementation after 16 weeks of supplementation (V3)
Liver fat content measured by MRI
Time frame: Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3)
Measurement of standard lipid profile
Time frame: Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3)
Measurement of glucose homeostasis
Time frame: Screening (V0), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3)
Cap score assessed by Fibroscan
Time frame: Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3)
Measurement of hs-CRP in mg /L Measurement of IL-6, MCP-1, RANTES in pg/ml
Time frame: Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3)
Measurement of BMI in kg/m²
Time frame: Baseline (V1) and End of supplementation after 16 weeks of supplementation (V3)
Evolution of body composition (i.e. total and trunk fat mass, total and trunk lean body mass) measured by Dual Energy X-ray Absorptiometry (DEXA)
Time frame: Baseline (V1) and End of supplementation after 16 weeks of supplementation (V3)
Health-related quality of life (HRQoF) assessed by Medical Outcome Study Short Form - 36 (MOS SF-36), a generic tool to measure and compare the HRQoL on study population.
Time frame: Screening (V0), Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3)
Measurement of liver assessment
Time frame: Screening (V0), Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3)
Measurement of kidney assessment
Time frame: Screening (V0), Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3)
Measurement of systolic and diastolic blood pressure in mmHg
Time frame: Screening (V0), Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3)
Measurement of white blood cells, red blood cells, number of platelets, amount of hemoglobin in the blood, hematocrit, mean red blood volume, mean hemoglobin amount per red blood cell, mean amount of hemoglobin relative to the size of the cell per red blood cell
Time frame: Screening (V0), Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3)
Measurement of thyroid stimulating hormone
Time frame: Screening (V0), Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3)
Treatment-Emergent Adverse Events (TEAE), Serious-TEAE (STEAE), TEAE leading to investigational product discontinuation, Treatment-Emergent Adverse Reaction (TEAR)
Interested in participating?
Request InfoValbiotis
Industry
A Parallel, Randomized, Placebo-Controlled, Double-Blinded Clinical Trial of the Effects of TOTUM-448 on Liver Fat Content, Cardiometabolic Risk Factors and Gut Microbiota Among Both Men and Women with MASLD
Acronym: CARDIO-LIVER
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06354088
Body Weight, Diabetes Mellitus
New York, United States
View Trial DetailsNCT07403604
Body Weight, Diabetes Mellitus
New York, United States
View Trial DetailsNCT06138821
Body Weight, Body Weight Changes
Boston, Massachusetts, United States
View Trial DetailsNCT06061042
Body Weight, Digestive System Diseases
Amsterdam, North Holland, Netherlands
View Trial Details