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临床试验/NCT01032941
NCT01032941已完成1 期

A Randomized Controlled Trial on the Beneficial Effects of Probiotics on Portal Hemodynamics in Decompensated Cirrhotic Patients

University of Alberta1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2009年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
18
试验地点
1
主要终点
Reduction in portal pressure

研究概览

简要总结

The investigators will address the hypothesis that portal hypertension is mediated in part by bacterial or endotoxin translocation and the production of inflammatory mediators (tumor necrosis factor-α (TNFα), etc.). The investigators hypothesize that food supplementation with the probiotic product VSL#3 in patients with Child Pugh B/C cirrhosis will have a beneficial effect on in portal pressure (as measured by the HVPG) by reducing inflammatory mediators and improving systemic and splanchnic hemodynamics.

详细描述

We have recently completed an open-label uncontrolled trial of the probiotic VSL#3 in 8 patients with compensated cirrhosis and evidence of portal hypertension (VIP study) to determine whether this agent would have beneficial effects in portal pressure reduction (unpublished data Tandon, P. et al.). The open label design and the inclusion of compensated (Child Pugh A) cirrhotic patients in this initial study were chosen to confirm the safety and tolerance of VSL#3 and the safety of the portal pressure measurements at our center. No changes of physical status occured. There was a non-significant reduction in portal pressure from 19.7 to 18.1 mm Hg after 2 months of VSL#3 supplementation. Furthermore, there was a significant reduction in the serum aldosterone level (p=0.03). IL-8 levels were reduced in 4/6 patients analyzed to date. These results suggest that VSL#3 results in cytokine reduction and an improvement in the effective circulating volume even in these well-compensated cirrhotic patients. The comparison of the rest of the pro-inflammatory mediators and stool microflora is still being analyzed.

The data in our initial study is very promising. As our patients were compensated cirrhotics with normal intestinal permeability and only mild baseline perturbations in hepatic function parameters (INR, bilirubin, albumin) and neurohormonal markers (aldosterone, renin), it is not surprising that a reduction in portal pressure was not identified. Consistent with previous studies however, these local results confirm the safety and tolerance of both VSL#3 as well as portal pressure measurements in cirrhotic patients (20,24,25).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-80
  • Cirrhosis
  • Childs-Pugh Class B/C

排除标准

  • Bacterial infection
  • Grade 3-4 hepatic encephalopathy
  • GI bleeding in the past 2 weeks
  • Hepatocellular carcinoma beyond the Milan criteria
  • Transjugular intrahepatic portosystemic shunt (TIPS), surgical shunt
  • Portal vein thrombosis
  • Antibiotics in the past 2 weeks
  • Myocardial infarction, stroke or life-threatening arrhythmia within the last 6 months
  • Active alcohol or illicit drug use
  • Failure to consent to the study

研究组 & 干预措施

Placebo

Placebo Comparator

Patients in this group will be given placebo 2 packets BID for 8 weeks.

干预措施: Probiotic (Drug)

VSL#3

Experimental

Patients in this group will be given 2 packets of VSL#3 BID for 8 weeks.

干预措施: Probiotic (Drug)

结局指标

主要结局

Reduction in portal pressure

时间窗: 12 months

次要结局

未报告次要终点

研究者

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

Puneeta Tandon

Assistant Professor

University of Alberta

研究点 (1)

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