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Metformin in Non-Alcoholic Fatty Liver Disease

Primary Purpose

Fatty Liver

Status
Unknown status
Phase
Phase 2
Locations
Norway
Study Type
Interventional
Intervention
metformin
Sponsored by
University Hospital, Aker
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fatty Liver focused on measuring hepatitis, metformin, non-alcoholic fatty liver (NAFLD), non-alcoholic steatohepatitis (NASH), Nonalcoholic fatty liver disease

Eligibility Criteria

20 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Histologically proven NAFLD less than 18 months prior to inclusion. For those with pure steatosis, ALAT or aspartate aminotransferase (ASAT) must be elevated above the upper limits of normal, and impaired glucose tolerance or diabetes mellitus type 2 must be present. Body weight within +/- 5 kg compared with the weight at the time of biopsy. Exclusion Criteria: Treatment for more than 1 week with metformin or glitazones the last 6 months before inclusion. Treatment with insulin. Hypersensitivity to metformin. Treatment with cimetidine. Heart failure requiring pharmacological treatment. Coronary heart disease (New York Heart Association [NYHA] class 3 or 4). Chronic obstructive lung disease (moderate or severe). Breast-feeding or pregnant. Metabolic acidosis. Renal failure (male [♂]: creatinine > 135 micromol/L, female [♀] > 110 micromol/L). Average alcohol consumption > 24 g/day the last year. Serum ALAT or serum ASAT > 5 x upper limit of normal (ULN) at screening. Cirrhosis. Platelets < 100 000. Haemochromatosis. Alfa-1-antitrypsin-deficiency. Wilson's disease. Thyroid dysfunction (0.2 mU/L < thyroid stimulating hormone [TSH] < 5.0 mU/L). Chronic infection with hepatitis B or C virus or HIV. Autoimmune hepatitis (antinuclear antibodies [ANA] > 1/256 or smooth muscle antibodies [SMA] > 1/128). Primary biliary cirrhosis (antimitochondrial antibodies [AMA] > 1/64). Primary sclerosing cholangitis. Previous participation in another clinical trial the last 6 months. Legal incapability.

Sites / Locations

  • Haukeland Universitetssykehus
  • Aker University Hospital
  • Akershus University Hospital
  • Universitetssykehuset i Nord-Norge

Outcomes

Primary Outcome Measures

Grade of steatosis as judged by repeat biopsy

Secondary Outcome Measures

Grade of necroinflammation as judged by repeat biopsy
Liver density obtained by computer scan
Serum alanine transaminase (ALAT)

Full Information

First Posted
March 16, 2006
Last Updated
June 29, 2007
Sponsor
University Hospital, Aker
Collaborators
Merck Sharp & Dohme LLC
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1. Study Identification

Unique Protocol Identification Number
NCT00303537
Brief Title
Metformin in Non-Alcoholic Fatty Liver Disease
Official Title
Double Blind, Randomized, Placebo Controlled Trial With Metformin in Non-Alcoholic Fatty Liver Disease (NAFLD)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2007
Overall Recruitment Status
Unknown status
Study Start Date
November 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2008 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
University Hospital, Aker
Collaborators
Merck Sharp & Dohme LLC

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study evaluates the use of the antidiabetic medicine metformin in nonalcoholic fatty liver disease.
Detailed Description
Nonalcoholic fatty liver disease (NAFLD) is a prevalent disorder associated with insulin resistance. Metformin is a drug that has been used for several decades in the treatment of diabetes mellitus. Metformin is known to improve insulin sensitivity. Some authors have reported beneficial effects of metformin in NAFLD, others have not been able to reproduce these findings. Only a few randomized controlled studies have been published so far, and there is still need for controlled trials with sufficient power to assess the efficacy of metformin in this condition. The aim of this study is to see whether treatment with metformin for 26 weeks results in reduction of liver steatosis (primary endpoint) and reduction in grade of inflammation in those with non-alcoholic steatohepatitis (NASH) (secondary endpoint).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fatty Liver
Keywords
hepatitis, metformin, non-alcoholic fatty liver (NAFLD), non-alcoholic steatohepatitis (NASH), Nonalcoholic fatty liver disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
metformin
Primary Outcome Measure Information:
Title
Grade of steatosis as judged by repeat biopsy
Time Frame
6 mo
Secondary Outcome Measure Information:
Title
Grade of necroinflammation as judged by repeat biopsy
Time Frame
6 mo
Title
Liver density obtained by computer scan
Time Frame
6 mo
Title
Serum alanine transaminase (ALAT)
Time Frame
6 mo

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically proven NAFLD less than 18 months prior to inclusion. For those with pure steatosis, ALAT or aspartate aminotransferase (ASAT) must be elevated above the upper limits of normal, and impaired glucose tolerance or diabetes mellitus type 2 must be present. Body weight within +/- 5 kg compared with the weight at the time of biopsy. Exclusion Criteria: Treatment for more than 1 week with metformin or glitazones the last 6 months before inclusion. Treatment with insulin. Hypersensitivity to metformin. Treatment with cimetidine. Heart failure requiring pharmacological treatment. Coronary heart disease (New York Heart Association [NYHA] class 3 or 4). Chronic obstructive lung disease (moderate or severe). Breast-feeding or pregnant. Metabolic acidosis. Renal failure (male [♂]: creatinine > 135 micromol/L, female [♀] > 110 micromol/L). Average alcohol consumption > 24 g/day the last year. Serum ALAT or serum ASAT > 5 x upper limit of normal (ULN) at screening. Cirrhosis. Platelets < 100 000. Haemochromatosis. Alfa-1-antitrypsin-deficiency. Wilson's disease. Thyroid dysfunction (0.2 mU/L < thyroid stimulating hormone [TSH] < 5.0 mU/L). Chronic infection with hepatitis B or C virus or HIV. Autoimmune hepatitis (antinuclear antibodies [ANA] > 1/256 or smooth muscle antibodies [SMA] > 1/128). Primary biliary cirrhosis (antimitochondrial antibodies [AMA] > 1/64). Primary sclerosing cholangitis. Previous participation in another clinical trial the last 6 months. Legal incapability.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kaare Birkeland, Prof./Ph.D
Organizational Affiliation
Aker University Hospital, Oslo, Norway
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Zbigniew Konopski, Cons./Ph.D
Organizational Affiliation
Aker University Hospital, Oslo, Norway
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Kristian Bjøro, Cons./Ph.D
Organizational Affiliation
Rikshospitalet-Radiumhospitalet, Oslo, Norway
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
John W Haukeland, Physician
Organizational Affiliation
University Hospital, Aker
Official's Role
Principal Investigator
Facility Information:
Facility Name
Haukeland Universitetssykehus
City
Bergen
Country
Norway
Facility Name
Aker University Hospital
City
Oslo
Country
Norway
Facility Name
Akershus University Hospital
City
Oslo
Country
Norway
Facility Name
Universitetssykehuset i Nord-Norge
City
Tromsø
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
22170794
Citation
Haukeland JW, Dahl TB, Yndestad A, Gladhaug IP, Loberg EM, Haaland T, Konopski Z, Wium C, Aasheim ET, Johansen OE, Aukrust P, Halvorsen B, Birkeland KI. Fetuin A in nonalcoholic fatty liver disease: in vivo and in vitro studies. Eur J Endocrinol. 2012 Mar;166(3):503-10. doi: 10.1530/EJE-11-0864. Epub 2011 Dec 14.
Results Reference
derived
PubMed Identifier
19811343
Citation
Haukeland JW, Konopski Z, Eggesbo HB, von Volkmann HL, Raschpichler G, Bjoro K, Haaland T, Loberg EM, Birkeland K. Metformin in patients with non-alcoholic fatty liver disease: a randomized, controlled trial. Scand J Gastroenterol. 2009;44(7):853-60. doi: 10.1080/00365520902845268.
Results Reference
derived

Learn more about this trial

Metformin in Non-Alcoholic Fatty Liver Disease

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