Resveratrol in Patients With Non-alcoholic Fatty Liver Disease (LIRMOI3)
Primary Purpose
Fatty Liver
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Resveratrol
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Fatty Liver focused on measuring Non-alcoholic Fatty Liver Disease, Non-alcoholic Steatohepatitis, Resveratrol, Human study
Eligibility Criteria
Inclusion Criteria:
- ALT ≥70 U/L for men and ≥45 U/L for women
- steatosis of the liver, assessed by ultrasonography
one of the following:
- waist circumference ≥102 cm for men and ≥88 for women
- hypertension: BP ≥130/80 mmHg
- raised triglycerides ≥1,7 mmol/L
- reduced HDL cholesterol ≤1.0 mmol/L
- BMI ≥ 25 kg/m²
Exclusion Criteria:
- weight > 130 kg
- comorbidity such as diabetes, cancer, metabolic or coagulation disorder, or significant liver-, heart- or kidney disease
- MRI contraindication
- treatment with glucocorticoids or methotrexate
- alcohol intake >20g/daily for men and >12 for women
Sites / Locations
- Aarhus University Hospital, Dept. of Hepatology and Gastroentology
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Resveratrol
Placebo
Arm Description
Subjects are given resveratrol 500 mg 3 times daily for 6 months.
Subjects are given Placebo tablets 3 times daily for 6 months.
Outcomes
Primary Outcome Measures
Change in hepatic steatosis and inflammation
Changes in hepatic and inflammatory markers ind the blood such as ALT, hs-CRP, TNFa Changes in hepatic fat content, assessed by MR spectroscopy Changes in hepatic steatosis and inflammation, assessed histologically Changes in the expression of proteins in the relevant inflammatory pathways, assessed by gene expression studies
Secondary Outcome Measures
Assessment of tolerability and side-effects
Assessment of tolerability and side-effects of Resveratrol versus placebo
Full Information
NCT ID
NCT01464801
First Posted
September 29, 2011
Last Updated
June 12, 2015
Sponsor
University of Aarhus
Collaborators
The Ministry of Science, Technology and Innovation, Denmark, Aarhus University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01464801
Brief Title
Resveratrol in Patients With Non-alcoholic Fatty Liver Disease
Acronym
LIRMOI3
Official Title
Long-term Investigation of Resveratrol on Management of Metabolic Syndrome, Osteoporosis and Inflammation, and Identification of Plant Derived Anti-inflammatory Compounds, Study 3
Study Type
Interventional
2. Study Status
Record Verification Date
August 2013
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
February 2015 (Actual)
Study Completion Date
June 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
Collaborators
The Ministry of Science, Technology and Innovation, Denmark, Aarhus University Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Non-alcoholic fatty liver disease (NAFLD) and fatty liver hepatitis (NASH) are very common in the Western world and strongly associated with obesity. No known effective treatment is known. From animal studies, it is known that the compound resveratrol perhaps has the potential to neutralize obesity-induced diseases. Resveratrol is already widely used as a food supplement though the precise effects are unknown. This project focuses on the effect of Resveratrol on fatty liver disease. The researchers plan to investigate the effects of Resveratrol or placebo treatment for 6 months on NAFLD/NASH in obese patients.
Detailed Description
Obesity is associated with non-alcoholic fatty liver disease (NAFLD) and steatohepatitis (NASH) and recently, low-grade inflammation has been hypothesized to be the causative link. From animal studies, it is known that the compound resveratrol (RES) has strong anti-inflammatory and antioxidant effects and perhaps the potential to neutralize obesity-induced diseases. RES is already widely used as a food supplement though the precise effects are unknown. This project focuses on the effect of RES on fatty liver disease. In a double-blind controlled clinical trial, the researchers investigate the effects of RES 500 mg or placebo treatment x 3 daily for 6 months on NAFLD/NASH in 48 obese patients in a double-blind, randomised, controlled clinical trial. The researchers hypothesize that RES improves the ALT levels and reduces liver fat and inflammation assessed by MR spectroscopy and histological evaluation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fatty Liver
Keywords
Non-alcoholic Fatty Liver Disease, Non-alcoholic Steatohepatitis, Resveratrol, Human study
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
28 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Resveratrol
Arm Type
Experimental
Arm Description
Subjects are given resveratrol 500 mg 3 times daily for 6 months.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Subjects are given Placebo tablets 3 times daily for 6 months.
Intervention Type
Dietary Supplement
Intervention Name(s)
Resveratrol
Intervention Description
Tablet Resveratrol 500 mg 3 times daily for 6 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Tablet Placebo 3 times daily for 6 months
Primary Outcome Measure Information:
Title
Change in hepatic steatosis and inflammation
Description
Changes in hepatic and inflammatory markers ind the blood such as ALT, hs-CRP, TNFa Changes in hepatic fat content, assessed by MR spectroscopy Changes in hepatic steatosis and inflammation, assessed histologically Changes in the expression of proteins in the relevant inflammatory pathways, assessed by gene expression studies
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Assessment of tolerability and side-effects
Description
Assessment of tolerability and side-effects of Resveratrol versus placebo
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
ALT ≥70 U/L for men and ≥45 U/L for women
steatosis of the liver, assessed by ultrasonography
one of the following:
waist circumference ≥102 cm for men and ≥88 for women
hypertension: BP ≥130/80 mmHg
raised triglycerides ≥1,7 mmol/L
reduced HDL cholesterol ≤1.0 mmol/L
BMI ≥ 25 kg/m²
Exclusion Criteria:
weight > 130 kg
comorbidity such as diabetes, cancer, metabolic or coagulation disorder, or significant liver-, heart- or kidney disease
MRI contraindication
treatment with glucocorticoids or methotrexate
alcohol intake >20g/daily for men and >12 for women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Henning Grønbæk, MD, PhD
Organizational Affiliation
Department of Hepatology and Gastroentology, Aarhus University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Aarhus University Hospital, Dept. of Hepatology and Gastroentology
City
Aarhus
ZIP/Postal Code
8000
Country
Denmark
12. IPD Sharing Statement
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Resveratrol in Patients With Non-alcoholic Fatty Liver Disease
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