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Administration of Probiotics in Cirrhotic Patients Listed for Liver Transplantation

Primary Purpose

Liver Cirrhosis

Status
Completed
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Placebo
Probiotic
Sponsored by
Medical University of Warsaw
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Liver Cirrhosis focused on measuring Liver cirrhosis, Liver transplantation, Probiotics, Mortality, Liver function, Infections

Eligibility Criteria

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

Inclusion Criteria:

  • Liver cirrhosis
  • Active status on the waiting list for liver transplantation
  • Confirmed etiology of liver disease

Exclusion Criteria:

  • Malignancy
  • Human Immunodeficiency Virus infection
  • Immunosuppressive treatment prior to liver transplantation
  • Cystic fibrosis
  • Creatinine clearance rate < 50 mL/min

Sites / Locations

  • Department of General, Transplant and Liver Surgery, Medical University of Warsaw

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Probiotic

Placebo

Arm Description

Capsules with 3x10^9 colony forming units (Lactococcus lactis PB 411 - 50%; Lactobacillus casei PB 121 - 25%; Lactobacillus acidophilus PB 111 - 12,5%; Bifidobacterium bifidum PB 211 - 12,5%). 1 capsule a day from inclusion until liver transplantation

Placebo, 1 capsule a day from inclusion until the date of liver transplantation

Outcomes

Primary Outcome Measures

All-cause postoperative mortality
Postoperative infection

Secondary Outcome Measures

Mortality on the waiting list
Infections in the pre-transplantation period
Primary non-function after liver transplantation
Changes in model for end-stage liver disease score
Changes in Child-Turcotte-Pugh class
Number of hospital admissions due to infections in the pre-transplantation period
Number of hospital admission due to complications of liver cirrhosis in the pre-transplantation period
Serum activity of transaminases on the first 5 postoperative days
Serum bilirubin concentration in the first 5 postoperative days
International normalized ratio values during the first 5 postoperative days
Change in model for end-stage liver disease score in the pre-transplantation period
To be assessed if the period between inclusion in the study and liver transplantation would not be shorter than 10 weeks
Change in Chil-Turcotte-Pugh class in the pre-transplantation period
To be assessed if the period between inclusion in the study and liver transplantation would not be shorter than 10 weeks

Full Information

First Posted
November 23, 2012
Last Updated
July 28, 2016
Sponsor
Medical University of Warsaw
Collaborators
Ministry of Science and Higher Education, Poland
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1. Study Identification

Unique Protocol Identification Number
NCT01735591
Brief Title
Administration of Probiotics in Cirrhotic Patients Listed for Liver Transplantation
Official Title
An Attempt to Optimize the Results of Liver Transplantation With Administration of Probiotics.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
November 2012 (undefined)
Primary Completion Date
November 2015 (Actual)
Study Completion Date
November 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medical University of Warsaw
Collaborators
Ministry of Science and Higher Education, Poland

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study was to evaluate the impact of the administration of probiotics on outcomes of patients qualified for liver transplantation, both in the pre-transplant period and in the early postoperative period.
Detailed Description
Gut microflora plays an important role in the pathogenesis of complications of liver cirrhosis, mainly due to microbial translocation. According to several studies, administration of probiotics in patients with cirrhosis has positive effect on minimal hepatic encephalopathy. The aim of this study was to evaluate the impact of probiotics administration on outcomes of patients qualified for liver transplantation, both in the pre-transplant period and in the early postoperative period. This study will be performed on 200 patients randomized into the probiotic and placebo groups. Daily administration of either probiotics or placebo will be continued from the date of inclusion in the study until the date of liver transplantation. A quantitative and qualitative analyses of faecal microflora will be performed in each patient before and after 10 week period (or shorter, depending on the time on the waiting list) of administration of either probiotic or placebo. Microbiological analyses of air samples from patients' home environment will be performed in each case. Both groups of patients will be compared with respect to primary and secondary outcome measures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cirrhosis
Keywords
Liver cirrhosis, Liver transplantation, Probiotics, Mortality, Liver function, Infections

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
55 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Probiotic
Arm Type
Experimental
Arm Description
Capsules with 3x10^9 colony forming units (Lactococcus lactis PB 411 - 50%; Lactobacillus casei PB 121 - 25%; Lactobacillus acidophilus PB 111 - 12,5%; Bifidobacterium bifidum PB 211 - 12,5%). 1 capsule a day from inclusion until liver transplantation
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo, 1 capsule a day from inclusion until the date of liver transplantation
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Placebo, 1 capsule a day from inclusion until the date of liver transplantation
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotic
Intervention Description
Capsules with 3x10^9 colony forming units of: Lactococcus lactis PB 411 (50%), Lactobacillus casei PB 121 (25%), Lactobacillus acidophilus PB 111 (12,5%), Bifidobacterium bifidum PB 211 (12,5)
Primary Outcome Measure Information:
Title
All-cause postoperative mortality
Time Frame
90 days after the date of liver transplantation
Title
Postoperative infection
Time Frame
30 days from the date of liver transplantation
Secondary Outcome Measure Information:
Title
Mortality on the waiting list
Time Frame
From the date of inclusion until the date of liver transplantation
Title
Infections in the pre-transplantation period
Time Frame
From the date of inclusion until the date of transplantation
Title
Primary non-function after liver transplantation
Time Frame
14 days after the date of liver transplantation
Title
Changes in model for end-stage liver disease score
Time Frame
From the date of inclusion until the date of transplantation
Title
Changes in Child-Turcotte-Pugh class
Time Frame
From the date of inclusion until the date of transplantation
Title
Number of hospital admissions due to infections in the pre-transplantation period
Time Frame
From the date of inclusion until the date of transplantation
Title
Number of hospital admission due to complications of liver cirrhosis in the pre-transplantation period
Time Frame
From the date of inclusion until the date of transplantation
Title
Serum activity of transaminases on the first 5 postoperative days
Time Frame
5 days after the date of liver transplantation
Title
Serum bilirubin concentration in the first 5 postoperative days
Time Frame
5 days after the date of liver transplantation
Title
International normalized ratio values during the first 5 postoperative days
Time Frame
5 days after the date of liver transplantation
Title
Change in model for end-stage liver disease score in the pre-transplantation period
Description
To be assessed if the period between inclusion in the study and liver transplantation would not be shorter than 10 weeks
Time Frame
10 weeks
Title
Change in Chil-Turcotte-Pugh class in the pre-transplantation period
Description
To be assessed if the period between inclusion in the study and liver transplantation would not be shorter than 10 weeks
Time Frame
10 weeks
Other Pre-specified Outcome Measures:
Title
Changes in faecal microflora
Description
Differences in the number of colony forming units in 1 g of stool for particular bacterial and fungal species after 10 weeks of probiotic/placebo administration
Time Frame
10 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Liver cirrhosis Active status on the waiting list for liver transplantation Confirmed etiology of liver disease Exclusion Criteria: Malignancy Human Immunodeficiency Virus infection Immunosuppressive treatment prior to liver transplantation Cystic fibrosis Creatinine clearance rate < 50 mL/min
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michał Grąt, M.D.
Organizational Affiliation
Medical University of Warsaw, Department of General, Transplant and Liver Surgery
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marek Krawczyk, Professor
Organizational Affiliation
Medical University of Warsaw, Department of General, Transplant and Liver Surgery
Official's Role
Study Chair
Facility Information:
Facility Name
Department of General, Transplant and Liver Surgery, Medical University of Warsaw
City
Warsaw
State/Province
Mazowieckie
ZIP/Postal Code
02-097
Country
Poland

12. IPD Sharing Statement

Citations:
PubMed Identifier
36126902
Citation
Cooper TE, Scholes-Robertson N, Craig JC, Hawley CM, Howell M, Johnson DW, Teixeira-Pinto A, Jaure A, Wong G. Synbiotics, prebiotics and probiotics for solid organ transplant recipients. Cochrane Database Syst Rev. 2022 Sep 20;9(9):CD014804. doi: 10.1002/14651858.CD014804.pub2.
Results Reference
derived
PubMed Identifier
33204004
Citation
Grat M, Grat K, Krawczyk M, Lewandowski Z, Krasnodebski M, Masior L, Patkowski W, Zieniewicz K. Post-hoc analysis of a randomized controlled trial on the impact of pre-transplant use of probiotics on outcomes after liver transplantation. Sci Rep. 2020 Nov 17;10(1):19944. doi: 10.1038/s41598-020-76994-3.
Results Reference
derived
PubMed Identifier
28506447
Citation
Grat M, Wronka KM, Lewandowski Z, Grat K, Krasnodebski M, Stypulkowski J, Holowko W, Masior L, Kosinska I, Wasilewicz M, Raszeja-Wyszomirska J, Rejowski S, Bik E, Patkowski W, Krawczyk M. Effects of continuous use of probiotics before liver transplantation: A randomized, double-blind, placebo-controlled trial. Clin Nutr. 2017 Dec;36(6):1530-1539. doi: 10.1016/j.clnu.2017.04.021. Epub 2017 May 4.
Results Reference
derived

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Administration of Probiotics in Cirrhotic Patients Listed for Liver Transplantation

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