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Omega 3 Supplementation in Fatty Liver (OMEGA 3 NASH)

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ClinicalTrials.gov Identifier: NCT01992809
Recruitment Status : Completed
First Posted : November 25, 2013
Last Update Posted : November 25, 2013
Information provided by (Responsible Party):

Study Description
Brief Summary:
Nonalcoholic fatty liver disease (NAFLD) is a clinical and pathological condition, whose spectrum can range from steatosis to steatohepatitis and cirrhosis, in patients without a history of alcohol abuse. Nonalcoholic steatohepatitis (NASH), the severe form of (NAFLD), has emerged as a clinically important type of chronic liver disease in industrialized countries and is characterized pathologically by hepatocellular ballooning, Mallory's hyaline, scattered inflammation and perisinusoidal fibrosis. NASH associated with cirrhosis can decompensate into subacute liver failure, progress to hepatocellular cancer and reoccur post transplantation.In the absence of established treatment, therapy is generally directed to treatment of risk factors for metabolic syndrome. Recently, some studies have been demonstrated that Polyunsaturated fatty acids (PUFAs), omega3 type, could reduced TNFalfa, IL6, aminotransferases, insulin resistance and steatosis verified by ultrasound. Neverthless, this is the first study that evaluate liver histology after six months of PUFA (omega3) in the treatment of patients with NASH.

Condition or disease Intervention/treatment Phase
Fatty Liver Dietary Supplement: Omega 3 Phase 3

  Show Detailed Description

Study Design

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 60 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Double (Care Provider, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Polyunsaturated Fatty Acid (Pufa) Omega 3 in the Reduction of the Inflammatory Component of the Nonalcoholic Steatohepatitis (Nash):Randomized Placebo Controlled Study
Study Start Date : September 2009
Primary Completion Date : June 2011
Study Completion Date : June 2011

Arms and Interventions

Arm Intervention/treatment
Active Comparator: Omega 3
Omega-3 group (n=30) received capsules containing 945 mg of Omega-3 PUFA [α linolenic acid/ 64%, eicosapentaenoic acid (EPA)/16% and docosahexaenoic acid (DHA)/21%], in 3 capsules/ day
Dietary Supplement: Omega 3
Omega-3 group (n=30) received capsules containing 945 mg of Omega-3 PUFA [α linolenic acid/ 64%, eicosapentaenoic acid (EPA)/16% and docosahexaenoic acid (DHA)/21%], in 3 capsules/ day
Placebo Comparator: placebo mineral oil
placebo mineral oil 3 ml/day

Outcome Measures

Primary Outcome Measures :
  1. Efficacy in reduce inflammatory component of NASH for NAS score [ Time Frame: 6 months ]
    Determine the efficacy of Omega-3 fatty acid in reducing the inflammatory component of NASH for liver through liver biopsy NAS score.

Secondary Outcome Measures :
  1. Inflammatory systemic profile [ Time Frame: 6 mothns ]
    Measure TNFalfa, IL6, adiponectin, lipidic leuckocyte profile, EPA (eicosapentaenoic acid), DHA (docosahexaenoic) and laboratory tests AST, ALT, Cholesterol, total triglycerides, PCR, VHS, SAA.

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 70 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • 18-70 years of age, both sexes
  • With or without non-insulin-dependent diabetes or glucose intolerance
  • Absence of alcoholism <20g (women) and <40g (men) of ethanol/day, drugs, schistosomiasis, hepatitis B or C and other chronic liver diseases cause determined
  • Absence of autoantibodies and rates of copper and ceruloplasmin normal
  • Biopsy-liver until 12 months previous, showing steatosis, lobular inflammatory infiltrate and ballooning of hepatocytes, which may be present or not Mallory's corpuscles and liver fibrosis stage I and II, NAS score> 5;
  • Patients who agree to participate in the study and all signed informed consent.

Exclusion Criteria:

  • Poisoning by exogenous oxidants
  • Pregnancy and lactation
  • Prothrombin time <70% or platelet count <70 000/mm3, or any bleeding disorders, including alteration of the bleeding time
  • Refusal to cooperate with research
  • steatosis without signs of inflammation or ballooning or cirrhosis (stage IV)
  • diabetes mellitus using insulin
  • allergy to fish or flaxseed
  • anti-inflammatory use of non-hormonal
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01992809

University of Sao Paulo School of Medicine
Sao Paulo, Brazil, 01246903
Sponsors and Collaborators
University of Sao Paulo General Hospital
Principal Investigator: CLAUDIA PM OLIVEIRA, MD, PhD University of Sao Paulo, School of Medicine
More Information

Responsible Party: Claudia Pinto Marques Oliveira, PhD, University of Sao Paulo General Hospital
ClinicalTrials.gov Identifier: NCT01992809     History of Changes
Other Study ID Numbers: 0681/09CAPPESQ
First Posted: November 25, 2013    Key Record Dates
Last Update Posted: November 25, 2013
Last Verified: November 2013

Keywords provided by Claudia Pinto Marques Oliveira, University of Sao Paulo General Hospital:
Nonalcoholic fatty liver
omega 3

Additional relevant MeSH terms:
Fatty Liver
Liver Diseases
Digestive System Diseases
Mineral Oil
Dermatologic Agents