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临床试验/NCT01565278
NCT01565278终止3 期

Effect of n-3 Polyunsaturated Fatty Acid Lipid Emulsion on Parenteral Nutrition Associated Liver Disease

Johane Allard4 个研究点 分布在 1 个国家目标入组 2 人开始时间: 2012年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
终止
发起方
入组人数
2
试验地点
4
主要终点
Response to treatment at 3 months

研究概览

简要总结

Patients who are not able to eat normally for a longer time require parenteral nutrition, i.e. they receive liquids and nutrients directly into their veins. This can have many long-term side effects, including liver problems. This study will examine whether a specific lipid emulsion containing fish oil can improve liver disease in patients on parenteral nutrition. The investigators will compare changes in bilirubin and liver enzymes after 3 months in 10 patients receiving standard lipid emulsion to 10 patients receiving standard lipids + a fish-oil containing emulsion. The investigators will also assess liver histology, the kind of fat, oxidative stress and gene expression in the liver at the beginning and after 6 months of fish-oil. The investigators also want to compare the baseline values from all 20 patients to 20 healthy controls. This will help to explain how fish oil may improve liver disease in patients on parenteral nutrition.

详细描述

Chronic exposure to total parenteral nutrition (TPN) can cause parenteral nutrition associated liver disease (PNALD), a progressive condition that may severely affect the liver and lead to end-stage liver disease. Fish oil has been shown to exert beneficial effects as it favorably alters metabolism and inflammation. It has been used parenterally (Omegaven) in young children with short bowel syndrome and PNALD with encouraging results. In adults it has mostly been used in peri-surgical settings as well as in critically ill patients, again proving its effectiveness.

The goal of this proposal is to show that Omegaven use in home-TPN patients with PNALD and elevated bilirubin despite conventional treatment, is beneficial in improving cholestasis and reducing intrahepatic inflammation. Primary objective is to compare the response to treatment between the Omegaven and the Intralipid group. Secondary objectives are to study the effect of Omegaven supplementation on single liver function tests, liver histology, liver fatty acid composition, liver oxidative stress and gene expression. In addition, the investigators want to compare the baseline values of all 20 patients to 20 healthy controls subjects.

After establishing that the patients' liver disease does not improve with conventional medical treatments for 3 months, as evidenced by repeated blood work at that time, they will all have a liver biopsy done as per diagnostic standards. They will then be randomized to either continue receiving Intralipid (0.25 g/kg/TPN day) or a mixture of Intralipid (0.25 g/kg/TPN day) and Omegaven (0.4 g/kg/TPN day) for a period of 3 months. After that, patients in the Omegaven arm will continue their treatment for 3 more months. Those in the Intralipid arm will be switched over to also receive Omegaven for the following 6 months.

Blood work will be repeated every 3 months after the initiation of the intervention. A repeat liver biopsy will be done in both groups after 6 months.

Main outcome is response to treatment (improvement in liver function tests) after 3 months (comparing Intralipid to Omegaven). In addition, change in liver function tests during the 6 months on Omegaven will be assessed. Lipid peroxidation and oxidative stress, fatty acid composition, and gene expression in the liver will be compared before and after 6 months on Omegaven.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Clinically stable patients on home TPN with PNALD with persistently elevated bilirubin (>1.5 times > normal) for at least 3 months despite standard treatment with ursodeoxycholic acid (15-30 mg/kg or at least 500 mg/d orally), changes in TPN (reduction to 25 kcal/kg/TPN day with Intralipid 0.25 g/kg) , and antibiotics (Metronidazole 500 mg bid and Ciprofloxacin 500 mg bid)
  • male or female,equal or over 18 years of age
  • on stable TPN regimen equal or over 3 days/week
  • on a stable drug regimen for equal or over 3 months prior to randomization, which will not changed for the study duration if these drugs are ursodeoxycholic acid given for PNALD or others affecting glucose and lipid metabolism

排除标准

  • Not receiving lipid emulsion as part of TPN
  • Allergy to fish, egg , soy, and peanuts
  • Liver disease of other etiology (e.g. excessive alcohol intake >20g/d, viral hepatitis, auto-immune or drug-induced, hemochromatosis, alfa 1-antitrypsin deficiency, Wilson's disease)
  • Complications of chronic liver disease, such as recurrent variceal bleeding, ascites, encephalopathy or any other reason contraindicating a liver biopsy
  • Severe hemorrhagic disorders
  • Sepsis - Inflammatory processes
  • Taking medications that precipitate steatohepatitis (e.g. corticosteroids, methotrexate, or amiodarone)
  • Pregnancy, lactation
  • Fluid restriction - Omegaven is more dilute than Intralipid.

研究组 & 干预措施

Soybean oil + Fish oil

Experimental

Intralipid (0.25 g/kg/TPN day) + Omegaven (0.4 g/kg/TPN day) for a period of 6 months.

干预措施: Soybean oil + Fish oil (Drug)

Soybean oil (Standard treatment)

Active Comparator

Standard treatment: Intralipid (0.25 g/kg/TPN day) for a period of 6 months

干预措施: Soybean oil (Standard treatment) (Drug)

结局指标

主要结局

Response to treatment at 3 months

时间窗: 3 months

Response is defined as improvement of at least one PNALD parameter by 20% or more; PNALD parameters are: ALP, GGT, ALT, total bilirubin Yes/No

次要结局

  • Changes in liver oxidative stress between baseline and 6 months(0, 6 months)
  • Change in total and conjugated bilirubin over time(0, 3, 6 months on Omegaven)
  • Changes in liver histology between baseline and 6 months on Omegaven(0, 6 months on Omegaven)
  • Changes in hepatic gene expression between baseline and 6 months on Omegaven(0, 6 months on Omegaven)
  • Changes in liver function test (ALP, AST, GGT) over 6 months(0, 3, 6 months on Omegaven)
  • Changes in liver fatty acid composition between baseline and 6 months on Omegaven(0, 6 months on Omegaven)

研究者

发起方
Johane Allard
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Johane Allard

Professor of Medicine, Gastroenterologist

University Health Network, Toronto

研究点 (4)

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