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临床试验/NCT05798702
NCT05798702进行中(未招募)不适用

Fibrosis Reduction in Non Alcoholic Steatohepatitis: the Effects of Weight Loss vs Metabolic Surgery

Fondazione Policlinico Universitario Agostino Gemelli IRCCS2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2021年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
20
试验地点
2
主要终点
histological reduction of fibrosis

研究概览

简要总结

Background: Non-Alcoholic Steatohepatitis (NASH) represents one of the stages of Non-Alcoholic Fatty Liver Disease (NAFLD) with a very high risk to evolve in cirrhosis and hepato-carcinoma.

Currently, the only diagnostic method is a liver biopsy that remains the gold standard for characterizing liver histologic alterations and fibrosis stages. There is no specific treatment for NASH, in fact no drugs are currently licensed specifically for treating this disease.

Aim: Our aim is to conduct a non-inferiority, randomized-controlled trial (RCT) comparing Roux-en-Y Gastric bypass (RYGB) with an intensive lifestyle modification plan (Very low-calorie diet, VLCD) for the reduction of advanced stages of fibrosis in subjects with obesity and NASH after 25% weight loss.

详细描述

Materials and Methods

The Investigators will screen patients with obesity, NAFLD fibrosis score (NFS) >0.676 and FibroScan > 9.5 kPA who have a high probability of NASH with advanced stage of fibrosis.

Participants will undergo liver biopsy to make diagnosis according to the Steatosis Activity Fibrosis (SAF) score algorithm. Subjects with BMI ≥ 30 and ≤50 kg/m2, age 25-65 years and F3-F4 fibrosis stage at liver biopsy will be included and randomized 1:1 to RYGB or VLCD. Anthropometric parameters, body composition with DEXA and liver function with blood samples will be assessed at the enrolment. A mixed meal metabolic test will be also performed to evaluate insulin sensitivity and secretion. These procedures will be repeated after 25% weight loss. Expectation: The Investigators expect a reduction of 2 points of histological fibrosis after 25% weight loss following either metabolic surgery or dieting. The investigators foresee also reversal of NASH, improvement of metabolic syndrome and glycemic control, changes in insulin sensitivity and secretion, changes in lipid profile, in NASH liver markers, in Fibroscan variables and in body composition

研究设计

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

入排标准

年龄范围
25 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Informed Consent signed before starting any procedure foreseen by the study;
  • Liver Ultrasound shoving steatosis and Fibroscan>9,5 KPa;
  • NAFLD fibrosis score>0,676;
  • diagnosis of NASH with stage F3-F4 of fibrosis according to SAF score, documented by liver biopsy and no evidence of another form of liver disease;
  • BMI≥ 30 and ≤50 kg/m2;
  • Age 25-65 years.

排除标准

  • Chronic liver disease other than NAFLD (e.g. hemochromatosis, viral or autoimmune hepatitis, Wilson's disease, α1 -antitrypsin deficiency);
  • Presence of esophageal varices and/or ascites;
  • INR ≥ 1,4;
  • Platelet count ≤ 100000;
  • Substantial alcohol consumption (>20 g/day for women or >30 g/day for men) and/or toxin exposure;
  • Coronary event or procedure (myocardial infarction, unstable angina, coronary artery bypass, surgery or coronary angioplasty) in the previous 6 months;
  • End stage renal failure;
  • Participation in any other concurrent therapeutic clinical trial;
  • Any other life-threatening, non-cardiac disease;
  • Pregnancy;
  • Type 1 diabetes, or LADA;
  • Lipodystrophy;
  • Abetalipoproteinemia;
  • Interfering medications (e.g., amiodarone, methotrexate, tamoxifen, corticosteroids);
  • Inability to give informed consent.

结局指标

主要结局

histological reduction of fibrosis

时间窗: 2 years

The primary outcome is the rate of histological reduction of 2 points of fibrosis after 25% weight loss following either metabolic surgery or dieting

次要结局

  • Liver histology(2 years)
  • Liver Markers(2 years)
  • Non-alcoholic Fatty Liver Disease Fibrosis score(2 years)
  • Fibrosis-4 (FIB-4) Index(2 years)
  • Fibroscan(2 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mingrone Geltrude

professor

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

研究点 (2)

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