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Pegylated-Interferon and Ribavirin Plus Metformin in the Treatment of Chronic HCV Infection and Insulin Resistance

Primary Purpose

Chronic Hepatitis C, Insulin Resistance

Status
Unknown status
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
metformin
Sponsored by
University of Turin, Italy
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Hepatitis C focused on measuring chronic hepatitis C, insulin resistance, therapy

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: No previous antiviral treatment Persistently elevated alanine aminotransferase (ALT) and quantifiable HCV-RNA (>2000 copies/ml) Liver biopsy (within 12 months) consistent with CHC with or without cirrhosis Compensated liver disease (Child-Pugh grade A) Insulin resistance (evaluated by HOMA-R and OGTT) Negative pregnancy test Exclusion Criteria: Type 2 Diabetes (according to ADA criteria) BMI > 30 Alcohol consumption > 30 g/day Other forms of liver disease (HBV, autoimmune, genetic), HIV infection. Anemia Psychiatric disease Thyroid disease poorly controlled Overt cirrhosis, hepatocellular carcinoma Significant cardiac, renal, pulmonary disease, seizures.

Sites / Locations

  • Division of Gastroenterology, University of Torino, Ospedale San Giovanni BattistaRecruiting

Outcomes

Primary Outcome Measures

Combined end-point of non-detectable serum HCV-RNA (<100 copies/mL) and
normal serum ALT activity at the end of the 24 week treatment-free follow up period

Secondary Outcome Measures

End-of-treatment virological and biochemical response
Sustained virological and biochemical response
End-of-treatment improvement of insulin resistance
End-of-treatment improvement of liver histology

Full Information

First Posted
August 30, 2006
Last Updated
November 13, 2006
Sponsor
University of Turin, Italy
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1. Study Identification

Unique Protocol Identification Number
NCT00370617
Brief Title
Pegylated-Interferon and Ribavirin Plus Metformin in the Treatment of Chronic HCV Infection and Insulin Resistance
Official Title
An Efficacy and Safety Study Comparing Pegylated-Interferon and Ribavirin Plus Metformin to Pegylated-Interferon and Ribavirin in the Treatment of naïve Patients With Genotype 1 Chronic HCV Infection and Insulin Resistance
Study Type
Interventional

2. Study Status

Record Verification Date
November 2006
Overall Recruitment Status
Unknown status
Study Start Date
September 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
January 2009 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
University of Turin, Italy

4. Oversight

5. Study Description

Brief Summary
Chronic hepatitis C virus (HCV) infection is associated with an increased risk for the development of type 2 diabetes and HCV infection itself may promote insulin resistance, irrespective of the severity of liver disease. Insulin resistance seems to be genotype specific and may play a role in fibrogenesis in chronic hepatitis C. In an "in vitro" model, increased levels of insulin may promote increased HCV replication. RATIONALE Decreased insulin resistance and reduced hyperinsulinemia may facilitate the efficacy of anti-viral drugs on HCV replication.
Detailed Description
Chronic hepatitis C virus (HCV) infection is associated with an increased risk for the development of type 2 diabetes and HCV infection itself may promote insulin resistance, irrespective of the severity of liver disease. In patients with HCV infection, an increase in fasting insulin levels is associated with the presence of serum HCV core, the severity of hepatic fibrosis and a decrease in expression of insulin receptor substrate (IRS) 1 and IRS2, central molecules of the insulin-signaling cascade. Down-regulation of IRS1 and IRS2 has also been observed in HCV core-transgenic mice livers and HCV core-transfected human hepatoma cells. High levels of tumor necrosis factor-alpha, which acts by disturbing tyrosine phosphorylation of insulin receptor substrate-1, may be associated with insulin resistance both in animal models and in HCV patients. Insulin resistance seems to be genotype specific and may play a role in fibrogenesis in chronic hepatitis C. In patients infected with genotype non-3, insulin resistance is associated with the degree of fibrosis, the rate of fibrosis progression and previous failed antiviral treatment. Insulin resistance, fibrosis, and genotype are independent predictors of the response to antiviral therapy in chronic hepatitis C patients treated with peginterferon plus ribavirin. A sustained virological response is achieved in 33% of patients with genotype 1 and insulin resistance compared with 60% of genotype 1 patients without insulin resistance. Insulin resistance is associated with a 3-fold risk of failure to antiviral treatment in patients with genotype 1 In an "in vitro" model, increased levels of insulin may promote increased HCV replication. RATIONALE Decreased insulin resistance and reduced hyperinsulinemia may facilitate the efficacy of anti-viral drugs on HCV replication. INDICATION Genotype 1 Chronic HCV hepatitis (CHC) associated with insulin resistance (IR). OBJECTIVES To compare the efficacy and safety of Pegylated-Interferon and Ribavirin plus metformin to Pegylated-Interferon and Ribavirin for treatment of naïve patients with Genotype 1 Chronic HCV infection and insulin resistance.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Hepatitis C, Insulin Resistance
Keywords
chronic hepatitis C, insulin resistance, therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
metformin
Primary Outcome Measure Information:
Title
Combined end-point of non-detectable serum HCV-RNA (<100 copies/mL) and
Title
normal serum ALT activity at the end of the 24 week treatment-free follow up period
Secondary Outcome Measure Information:
Title
End-of-treatment virological and biochemical response
Title
Sustained virological and biochemical response
Title
End-of-treatment improvement of insulin resistance
Title
End-of-treatment improvement of liver histology

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: No previous antiviral treatment Persistently elevated alanine aminotransferase (ALT) and quantifiable HCV-RNA (>2000 copies/ml) Liver biopsy (within 12 months) consistent with CHC with or without cirrhosis Compensated liver disease (Child-Pugh grade A) Insulin resistance (evaluated by HOMA-R and OGTT) Negative pregnancy test Exclusion Criteria: Type 2 Diabetes (according to ADA criteria) BMI > 30 Alcohol consumption > 30 g/day Other forms of liver disease (HBV, autoimmune, genetic), HIV infection. Anemia Psychiatric disease Thyroid disease poorly controlled Overt cirrhosis, hepatocellular carcinoma Significant cardiac, renal, pulmonary disease, seizures.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mario Rizzetto, MD
Phone
+39-011-6336397
Email
mrizzetto@molinette.piemonte.it
First Name & Middle Initial & Last Name or Official Title & Degree
Elisabetta Bugianesi, MD
Phone
+39-011-6336397
Email
ebugianesi@yahoo.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mario Rizzetto, MD
Organizational Affiliation
University of Torino
Official's Role
Principal Investigator
Facility Information:
Facility Name
Division of Gastroenterology, University of Torino, Ospedale San Giovanni Battista
City
Torino
ZIP/Postal Code
10126
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mario Rizzetto, MD
Phone
+39-011-6336397
Email
mrizzetto@molinette.piemonte.it
First Name & Middle Initial & Last Name & Degree
Elisabetta Bugianesi, MD
Phone
+39-011-6336397
Email
ebugianesi@yahoo.it
First Name & Middle Initial & Last Name & Degree
Elisabetta Bugianesi, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
15765399
Citation
Romero-Gomez M, Del Mar Viloria M, Andrade RJ, Salmeron J, Diago M, Fernandez-Rodriguez CM, Corpas R, Cruz M, Grande L, Vazquez L, Munoz-De-Rueda P, Lopez-Serrano P, Gila A, Gutierrez ML, Perez C, Ruiz-Extremera A, Suarez E, Castillo J. Insulin resistance impairs sustained response rate to peginterferon plus ribavirin in chronic hepatitis C patients. Gastroenterology. 2005 Mar;128(3):636-41. doi: 10.1053/j.gastro.2004.12.049.
Results Reference
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Pegylated-Interferon and Ribavirin Plus Metformin in the Treatment of Chronic HCV Infection and Insulin Resistance

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