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| Name | Class |
|---|---|
| CHU de Quebec-Universite Laval | OTHER |
| Institut universitaire de cardiologie et de pneumologie de Québec, University Laval | OTHER |
| Laval University | OTHER |
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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| TOTUM-448 | Experimental | The experimental active arm will be supplemented with TOTUM-448 twice per day. |
|
| Placebo | Placebo Comparator | The placebo comparator arm will be supplemented with a placebo twice per day. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| TOTUM-448 | Dietary Supplement | 16 weeks of TOTUM-448 supplementation (4.284g/day corresponding to 8 capsules per day) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Evolution of liver fat content | Liver fat content measured by MRI | Baseline (V1) and End of supplementation after 16 weeks of supplementation (V3) |
| Measure | Description | Time Frame |
|---|---|---|
| Evolution of lipid profile | Measurement of standard lipid profile | Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3) |
| Evolution of glucose homeostasis |
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Main Inclusion Criteria:
Main Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Véronique Sapone, MSc | Contact | +33 (0)6 75 32 66 59 | veronique.sapone@valbiotis.com |
| Name | Affiliation | Role |
|---|---|---|
| André Marette, PhD | Laval University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Institut sur la nutrition et les aliments fonctionnels (INAF) | Recruiting | Québec | Quebec | G1V 0A6 | Canada |
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| ID | Term |
|---|---|
| D065626 | Non-alcoholic Fatty Liver Disease |
| D050177 | Overweight |
| D009765 | Obesity |
| D007333 | Insulin Resistance |
| ID | Term |
|---|---|
| D005234 | Fatty Liver |
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
| D044343 | Overnutrition |
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| Valbiotis Canada inc. |
| UNKNOWN |
Randomized, double-blinded, parallel, placebo-controlled study.
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| Placebo | Dietary Supplement | 16 weeks of placebo supplementation (8 capsules per day) |
|
Measurement of glucose homeostasis
| Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3) |
| Evolution of liver health | Cap score assessed by Fibroscan | Screening (V0), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3) |
| Evolution of inflammation | Measurement of hs-CRP in mg /L Measurement of IL-6, MCP-1, RANTES in pg/ml | Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3) |
| Evolution of anthropometric variables | Measurement of BMI in kg/m² | Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3) |
| Evolution of body composition | 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) | Baseline (V1) and End of supplementation after 16 weeks of supplementation (V3) |
| Evolution of health-related quality of life | 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. | Baseline (V1) and End of supplementation after 16 weeks of supplementation (V3) |
| Evolution of hepatic function | Measurement of liver assessment | Screening (V0), Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3) |
| Evolution of kidney function | Measurement of kidney assessment | Screening (V0), Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3) |
| Evolution of hemodynamic measurements | Measurement of systolic and diastolic blood pressure in mmHg | Screening (V0), Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3) |
| Evolution of complete blood count | 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 | Screening (V0), Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3) |
| Evolution of thyroid stimulating hormone | Measurement of thyroid stimulating hormone | Screening (V0), Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3) |
| Evolution of adverse events (TEAE, STEAE, TEAE leading to investigational product discontinuation, TEAR) | Treatment-Emergent Adverse Events (TEAE), Serious-TEAE (STEAE), TEAE leading to investigational product discontinuation, Treatment-Emergent Adverse Reaction (TEAR) | Screening (V0), Baseline (V1), Following 8 weeks of supplementation (V2) and End of supplementation after 16 weeks of supplementation (V3) |
| D009748 |
| Nutrition Disorders |
| D009750 | Nutritional and Metabolic Diseases |
| D001835 | Body Weight |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D006946 | Hyperinsulinism |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |