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Clinical Trial of Pentoxifylline in Patient With Cirrhosis

Phase 3
Completed
Conditions
Cirrhosis
Liver Failure
Interventions
Registration Number
NCT00162552
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

In patients with cirrhosis and liver failure, pro-inflammatory cytokines (TNF alpha) might be responsible of severe complications and death. Thus, the prevention of cytokine production should prevent complications and mortality.

The aim of this study is to study the 2 months survival rate in patients with severe cirrhosis (Child-Pugh C) with pentoxifylline - an inhibitor of cytokine production. The 6 month mortality, the proportion of transplanted patients, the occurrence of complications (bacterial infection, renal failure, hepatic encephalopathy and gastrointestinal bleeding), plasma cytokine levels and fibrotest - a marker of fibrosis - will be also studied. This is a multicenter double blind randomized trial with a placebo.

All adult patients with severe cirrhosis might be randomized after written consent. Patients with severe carcinoma, intolerance or contraindication to pentoxifylline will not be included. Patients receive either pentoxifylline or placebo 3 times a day for 6 months. Three hundred and forty two patients are necessary to decrease mortality rate by 50% at 2 months in a beta risk of 10% and an alpha risk of 5%. Patients will be seen every month.

Detailed Description

The aim of this study is to study the 2 months survival rate in patients with severe cirrhosis (Child-Pugh C) with pentoxifylline - an inhibitor of cytokine production. The 6 month mortality, the proportion of transplanted patients, the occurrence of complications (bacterial infection, renal failure, hepatic encephalopathy and gastrointestinal bleeding), plasma cytokine levels and fibrotest - a marker of fibrosis - will be also studied. This is a multicenter double blind randomized trial with a placebo.

All adult patients with severe cirrhosis might be randomized after written consent. Patients with severe carcinoma, intolerance or contraindication to pentoxifylline will not be included. Patients receive either pentoxifylline or placebo 3 times a day for 6 months. Three hundred and forty two patients are necessary to decrease mortality rate by 50% at 2 months in a beta risk of 10% and an alpha risk of 5%. Patients will be seen every month.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
342
Inclusion Criteria
  • adult patient of more than 18 years
  • child pugh C cirrhosis
Exclusion Criteria
  • pregnant woman
  • Patient received anticoagulant
  • Patient treated for arterial hypertension
  • Patient with severe coronaropathy
  • Patient with hyper sensibility of pentoxifylline
  • Patient hospitalized for less 24 hours
  • Patient admitted for a treatment of hepatocellular-carcinoma or COLLANGIO- carcinoma
  • Patient with HIV
  • Patient who has been transplanted
  • Patient treated with immuno- suppressors
  • Patient who has already received pentoxifylline for 3 months before inclusion
  • Patient for whom the follow-up is considered impossible

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1pentoxifyllinePatients with severe cirrhosis treated with Pentoxifylline
2PLACEBOPatients with severe cirrhosis treated with a placebo
Primary Outcome Measures
NameTimeMethod
survival rate at 2 monthsat 2 months
Secondary Outcome Measures
NameTimeMethod
- survival rate at 6 monthsat six months
- Number of patient with liver transplantationduring the study
- Complications : bacterial infection, renal insufficiency, hepatic encephalopathy, gastrointestinal bleedingduring the study
- Fibrotest and Acutest before, at 2 months and at 6 monthsat 2 months and at 6 months
- TNF alpha and IL6 plasma concentration before, at 2 months and at 6 months as predictive factor of mortalityat 2 months and at 6 months as predictive factor of mortality

Trial Locations

Locations (1)

Hôpital Beaujon

🇫🇷

Clichy, France

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