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Rifaximin vs Placebo for the Prevention of Encephalopathy in Patients Treated by TIPS (PRPET)

Primary Purpose

Cirrhosis

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Rifaximin
placebo
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cirrhosis focused on measuring TIPS, portal pressure, rifaximin, overt hepatic encephalopathy, microbiota

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • cirrhosis with TIPS for ascit treatment or hydrothorax
  • prevention digestive bleeding follow up portal hypertension -
  • signed consent

Exclusion Criteria:

  • hepatocellular carcinoma out of Milan criteria or palliative phase cancer
  • Child Pugh score > 12
  • TIPS indicated for other indication than bellow
  • encephalopathy signs : asterixis or confusion
  • Hypersensibility to rifaximin, or derivated of rifamycin
  • Patients treated by same class antibacterial
  • pregnant woman
  • Patient with hepatic transplant

Sites / Locations

  • CHU Angers
  • Hôpital Jean Verdier
  • CHU Bordeaux
  • CHRU Lille
  • CHU Marseille
  • CHU Nantes
  • CHU Beaujon Clichy
  • CHU Saint-Antoine
  • Pitié Salpêtrière
  • CHU Poitiers
  • CHU Rennes
  • UHToulouse
  • CHU Tours

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

rifaximin

placebo

Arm Description

6 rifaximin caps of 200 mg per day morning and night, during 15 days before TIPS, and after TIPS during 6 months.

6 caps placebo morning and night, 15 days before and 6 months after TIPS

Outcomes

Primary Outcome Measures

First episode of overt encephalopathy in patients treated by TIPS
First episode of overt encephalopathy in patients treated by TIPS

Secondary Outcome Measures

number of hospitalisation days
Number and days of hospitalisations for encephalopathy
Frequency of kidney insufficiency
number of digestive bleeding follow up to portal hypertension, number of ascit punctions, frequency kidney insufficiency and hepatocellular carcinoma
transplants, deaths
- number of transplants and deaths
intestinal microbiota
Composition of intestinal microbiota in 30 patients (only UHToulouse)

Full Information

First Posted
December 13, 2013
Last Updated
April 21, 2020
Sponsor
University Hospital, Toulouse
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1. Study Identification

Unique Protocol Identification Number
NCT02016196
Brief Title
Rifaximin vs Placebo for the Prevention of Encephalopathy in Patients Treated by TIPS
Acronym
PRPET
Official Title
Double Blind Randomized Study, Comparing Rifaximin vs Placebo for the Prevention of Encephalopathy in Patients Treated by TIPS
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
September 2013 (Actual)
Primary Completion Date
July 2017 (Actual)
Study Completion Date
July 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
TIPS has been used for 20 years, as a means of reducing portal pressure in patients with cirrhosis and portal hypertension related complications. TIPS proved more effective than alternative treatments in controlling or preventing variceal bleeding and refractory ascites. The main drawback of the TIPS procedure is progressive overt hepatic encephalopathy (OHE). Three risk factors for post-TIPS OHE have been identified: age over 65 years, history of previous episodes of OHE, and Child-Pugh score equal to or over 10. However, the incidence of post-TIPS OHE in patients fulfilling these criteria remains close to 35 %.
Detailed Description
TIPS has been used for 20 years, as a means of reducing portal pressure in patients with cirrhosis and portal hypertension related complications. TIPS proved more effective than alternative treatments in controlling or preventing variceal bleeding and refractory ascites. The main drawback of the TIPS procedure is progressive overt hepatic encephalopathy (OHE). Three risk factors for post-TIPS OHE have been identified: age over 65 years, history of previous episodes of OHE, and Child-Pugh score equal to or over 10. However, the incidence of post-TIPS OHE in patients fulfilling these criteria remains close to 35 %. Furthermore, the pathogenesis of HE in general but also in patients treated by TIPS is still not well understood. Therefore, there is a real challenge in discovering new molecular mechanisms involved in pathogenesis of OHE as well as new treatment to better prevent the risk of OHE in patients treated by TIPS. Observational and experimental studies suggest a microbiota's role in the mechanism of OHE and recently a non absorbable antibiotic has proven to reduce the risk of recurrence of OHE. However, the effect of this drug for the prevention of a first episode of OHE in patients treated by TIPS is not known. In addition, the mechanisms of the beneficial effect of rifaximin remain poorly understood.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cirrhosis
Keywords
TIPS, portal pressure, rifaximin, overt hepatic encephalopathy, microbiota

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
211 (Actual)

8. Arms, Groups, and Interventions

Arm Title
rifaximin
Arm Type
Experimental
Arm Description
6 rifaximin caps of 200 mg per day morning and night, during 15 days before TIPS, and after TIPS during 6 months.
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
6 caps placebo morning and night, 15 days before and 6 months after TIPS
Intervention Type
Drug
Intervention Name(s)
Rifaximin
Other Intervention Name(s)
NORMIX
Intervention Description
6 rifaximin caps of 200 mg morning and night, 15 days before and 6 months after TIPS --------------------------------------------------------------------------------
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
6 placebo caps per day morning and night, during 15 days before TIPS and 6 months after TIPS
Primary Outcome Measure Information:
Title
First episode of overt encephalopathy in patients treated by TIPS
Description
First episode of overt encephalopathy in patients treated by TIPS
Time Frame
6 months
Secondary Outcome Measure Information:
Title
number of hospitalisation days
Description
Number and days of hospitalisations for encephalopathy
Time Frame
6 months
Title
Frequency of kidney insufficiency
Description
number of digestive bleeding follow up to portal hypertension, number of ascit punctions, frequency kidney insufficiency and hepatocellular carcinoma
Time Frame
6 months
Title
transplants, deaths
Description
- number of transplants and deaths
Time Frame
6 months
Title
intestinal microbiota
Description
Composition of intestinal microbiota in 30 patients (only UHToulouse)
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: cirrhosis with TIPS for ascit treatment or hydrothorax prevention digestive bleeding follow up portal hypertension - signed consent Exclusion Criteria: hepatocellular carcinoma out of Milan criteria or palliative phase cancer Child Pugh score > 12 TIPS indicated for other indication than bellow encephalopathy signs : asterixis or confusion Hypersensibility to rifaximin, or derivated of rifamycin Patients treated by same class antibacterial pregnant woman Patient with hepatic transplant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christophe Bureau, MD PhD
Organizational Affiliation
University Hospital, Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Angers
City
Angers
Country
France
Facility Name
Hôpital Jean Verdier
City
Bondy
Country
France
Facility Name
CHU Bordeaux
City
Bordeaux
Country
France
Facility Name
CHRU Lille
City
Lille
Country
France
Facility Name
CHU Marseille
City
Marseille
Country
France
Facility Name
CHU Nantes
City
Nantes
Country
France
Facility Name
CHU Beaujon Clichy
City
Paris
Country
France
Facility Name
CHU Saint-Antoine
City
Paris
Country
France
Facility Name
Pitié Salpêtrière
City
Paris
Country
France
Facility Name
CHU Poitiers
City
Poitiers
Country
France
Facility Name
CHU Rennes
City
Rennes
Country
France
Facility Name
UHToulouse
City
Toulouse
ZIP/Postal Code
31059
Country
France
Facility Name
CHU Tours
City
Tours
Country
France

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
33524293
Citation
Bureau C, Thabut D, Jezequel C, Archambeaud I, D'Alteroche L, Dharancy S, Borentain P, Oberti F, Plessier A, De Ledinghen V, Ganne-Carrie N, Carbonell N, Rousseau V, Sommet A, Peron JM, Vinel JP. The Use of Rifaximin in the Prevention of Overt Hepatic Encephalopathy After Transjugular Intrahepatic Portosystemic Shunt : A Randomized Controlled Trial. Ann Intern Med. 2021 May;174(5):633-640. doi: 10.7326/M20-0202. Epub 2021 Feb 2.
Results Reference
derived

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Rifaximin vs Placebo for the Prevention of Encephalopathy in Patients Treated by TIPS

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