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Effects of Proteins in Patients With Cirrhosis and Prior Hepatic Encephalopathy

Phase 4
Completed
Conditions
Hepatic Encephalopathy
Interventions
Dietary Supplement: Maltodextrin
Dietary Supplement: Branched-chain amino acids
Registration Number
NCT00955500
Lead Sponsor
Hospital Universitari Vall d'Hebron Research Institute
Brief Summary

The purpose of this study is to compare a normal-protein diet containing branched-chain amino acids to a low-protein diet in patients with non-terminal cirrhosis (MELD \< 25) who have developed an episode of hepatic encephalopathy within two months prior to inclusion.

Detailed Description

Hepatic encephalopathy is a major complication of cirrhosis associated with poor prognosis and poor quality of life. Appearance of HE occurs in the setting of precipitating factors that increase plasma ammonia. The gastrointestinal tract is the primary source of ammonia, which is produced by enterocytes from glutamine and by colonic bacterial catabolism of nitrogenous sources, such as ingested proteins. This is the rationale for proposing low-protein diet as strategy to reduce ammonia production and as standard diet in patients with cirrhosis and hepatic encephalopathy. However, low-protein diet could cause wasting muscle and predispose to recurrence of hepatic encephalopathy, since muscle is an important site for extrahepatic ammonia removal.

Branched-chain amino acids have shown beneficial effects on mental state of patients with chronic hepatic encephalopathy. The possible mechanism of action may be improvement of nutritional status through induction of protein synthesis. However, role of branched-chain amino acids in treatment and prevention of acute hepatic encephalopathy is not established.

Administration of a normal-protein diet containing oral branched-chain amino acids may reduce recurrence of hepatic encephalopathy as compared to a low-protein diet.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
116
Inclusion Criteria
  • Cirrhosis of the liver.
  • Recovery from an episode of hepatic encephalopathy within two months prior to inclusion.
  • Compliance with a standard diet during two weeks prior to inclusion.
Exclusion Criteria
  • End-stage cirrhosis (MELD score > 25).
  • Marked cognitive disorder (mini-mental test < 27).
  • Non-treatable hepatocarcinoma in accordance with Milan criteria.
  • Comorbid conditions with a life expectancy less than 6 months.
  • Neurological conditions that difficult assessment of treatment of hepatic encephalopathy (dementia, encephalitis, severe depression).
  • Diseases requiring administration of a specific diet (malabsorption, chronic diarrhea, chronic pancreatic insufficiency, severe obesity).
  • No acceptation of written consent.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Low-protein dietMaltodextrinDaily diet containing 35 kcal/kg/day, 0.7 grams of proteins/kg/day + 30 grams of oral maltodextrine
Normal-protein dietBranched-chain amino acidsDaily diet containing 35 kcal/kg/day, 0.7 grams of proteins/kg/day + 30 grams of oral branched-chain amino acids (leucine: 13.5 grams, isoleucine: 9 grams, valine: 7.5 grams).
Primary Outcome Measures
NameTimeMethod
Hepatic encephalopathy-free survival56 weeks
Secondary Outcome Measures
NameTimeMethod
Nutritional status56 weeks
Minimal hepatic encephalopathy assessed by neuropsychological tests56 weeks
Overall duration in days of episodic hepatic encephalopathy56 weeks
Health-related quality of life56 weeks
Liver function56 weeks

Trial Locations

Locations (3)

Corporació Sanitària Parc Taulí

🇪🇸

Sabadell, Barcelona, Spain

Hospital del Mar

🇪🇸

Barcelona, Spain

Hospital de Sant Pau

🇪🇸

Barcelona, Spain

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