Use of Omega-3 Fatty Acids (Fish Oil) in Patients With Chronic Hepatitis C Infection
NCT ID: NCT00547716
Last Updated: 2017-01-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
NA
INTERVENTIONAL
2009-06-30
2012-08-31
Brief Summary
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The accumulation of fat in the liver has been blamed on a particular type of fat called triglycerides. Fish oil, by reducing a type of fat called VLDL, can lower the triglyceride concentration by as much as 50 percent or more. This study seeks to determine if the administration of fish oil along with standard treatment to patients with Hepatitis C will increase the treatment response rates.
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Detailed Description
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The pathogenesis of hepatic steatosis in chronic Hepatitis C infection has not been fully elucidated. Hepatic steatosis is a manifestation of excessive triglyceride accumulation in the liver. Hypertriglyceridemia may benefit from Omega-3 fatty acid (fish oil supplements) which, by reducing VLDL production can lower the serum triglyceride concentration by as much as 50 percent or more.
The treatment of chronic hepatitis C results in an average sustained viral response rate of 54%-63%. We have found response rates of around 50% on treatment of patients. We hypothesize that by giving omega-3 fatty acids along with interferon therapy for patients with Hepatitis C, we may be able to increase the treatment response rates. Thus, the purpose of the study is to look at the effect of omega 3 fatty acids on early and sustained viral response rates in patients with chronic HCV infection.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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1.
Omega-3 Fatty Acids 4 grams/day
Omega-3 Fatty Acids
Omega-3 Fatty Acids - 4 grams per day
2.
Placebo comparator along with interferon.
Placebo comparator
Interventions
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Omega-3 Fatty Acids
Omega-3 Fatty Acids - 4 grams per day
Placebo comparator
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Patients with chronic hepatitis C infection
* Patients receiving interferon for treatment of hepatitis C
Exclusion Criteria
* End stage target organ damage in diabetes mellitus: advanced renal failure (serum creatinine \>2.0 mg/dl) with or without dialysis, severe neuropathy, advanced peripheral vascular disease.
* Anticipated life expectancy less than 2 years
* Co-existent etiologies for liver disease
* Alcohol consumption more than 30 g per day in men and more than 20 g per day in women.
* Patients on Omega-3 fatty acid supplementation or those patients who report eating oily fish such as salmon, albacore tuna, sardines, etc. twice a week or more frequently.
18 Years
ALL
No
Sponsors
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Reliant Pharmaceuticals
INDUSTRY
Saint Luke's Health System Foundation
UNKNOWN
Truman Medical Center
OTHER
University of Missouri, Kansas City
OTHER
Responsible Party
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Principal Investigators
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Laura M Alba, M.D.
Role: PRINCIPAL_INVESTIGATOR
Truman Medical Center
Jagdish Nachnani, MD
Role: PRINCIPAL_INVESTIGATOR
Truman Medical Center
Locations
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Truman Medical Center
Kansas City, Missouri, United States
Saint Luke's Hospital
Kansas City, Missouri, United States
Countries
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Related Links
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Hepatitis information
Other Identifiers
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07-48
Identifier Type: -
Identifier Source: org_study_id
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