Rifaximin to Prevent Recurrent HCV-Related Fibrosis After Liver Transplant
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Hepatitis |
| Therapuetic Areas: | Immunology / Infectious Diseases |
| Healthy: | No |
| Age Range: | 18 - 70 |
| Updated: | 4/23/2016 |
| Start Date: | March 2012 |
| End Date: | December 2018 |
Prospective Randomized Double Blind Placebo Controlled Trial of Rifaximin 550mg PO Twice Daily for Three Months to Prevent Recurrent Fibrosis in Liver Transplant Recipients With Chronic Hepatitis C Virus Infection
The purpose of this study is to determine if the administration of a poorly-absorbable
antibiotic (rifaximin) for the first three months after liver transplant will reduce the
amount of fibrosis (or scarring of the liver) in liver transplant patients with recurrent
hepatitis C virus (HCV) by lowering serum lipopolysaccharide (LPS), a protein in blood that
comes from the bacteria in intestines and may cause scarring in the liver.
Approximately 60 subjects will participate in this study. Subjects will be part of the study
for approximately 1 year post transplant.
antibiotic (rifaximin) for the first three months after liver transplant will reduce the
amount of fibrosis (or scarring of the liver) in liver transplant patients with recurrent
hepatitis C virus (HCV) by lowering serum lipopolysaccharide (LPS), a protein in blood that
comes from the bacteria in intestines and may cause scarring in the liver.
Approximately 60 subjects will participate in this study. Subjects will be part of the study
for approximately 1 year post transplant.
Hepatitis C virus (HCV) is the most common chronic liver infection and remains the leading
indication for liver transplantation (LT). Although LT is a cure for cirrhosis of the liver,
it does not always cure HCV infection or reinfection of post-transplanted liver. Post-LT
recurrent HCV can lead to accelerated liver fibrosis. Chronic exposure to lipopolysaccharide
(LPS) from gut-derived bacteria has shown to be at elevated levels in patients with
cirrhosis due to HCV compared to normal controls. Therefore, the investigators hypothesize
that LPS contributes to cause of liver fibrosis, specifically in patients with post-LT
recurrent HCV, and this effect maybe modified with the poorly absorbed antibiotic,
rifaximin, which alter the gut flora of the patients.
indication for liver transplantation (LT). Although LT is a cure for cirrhosis of the liver,
it does not always cure HCV infection or reinfection of post-transplanted liver. Post-LT
recurrent HCV can lead to accelerated liver fibrosis. Chronic exposure to lipopolysaccharide
(LPS) from gut-derived bacteria has shown to be at elevated levels in patients with
cirrhosis due to HCV compared to normal controls. Therefore, the investigators hypothesize
that LPS contributes to cause of liver fibrosis, specifically in patients with post-LT
recurrent HCV, and this effect maybe modified with the poorly absorbed antibiotic,
rifaximin, which alter the gut flora of the patients.
Inclusion Criteria:
- Subject must provide written informed consent before any study assessment is
performed
- Age ≥ 18 years
- Willing and able to sign informed consent
- Chronic HCV infection with viremia
- Listed for liver transplantation
- Demonstrate ability to take oral medications prior to randomization (post LT)
Exclusion Criteria:
- Age < 18 years old
- Unwilling/able to sign informed consent
- Cleared HCV infection (and therefore not at risk for recurrent HCV)
- Human immunodeficiency virus (HIV) co-infection
- Hepatitis B (HBV) co-infection
- Participation in another interventional clinical trial
- Females of childbearing (reproductive) potential must have a negative serum pregnancy
test at Screening and agree to use an acceptable method of contraception throughout
their participation in the study
- Subjects with history of hypersensitivity to rifaximin, rifampin, rifamycin
antimicrobial agents, or any of the components of rifaximin
- Subjects with history of tuberculosis infection or has received treatment for
tuberculosis infection. If subject has previous positive test for tuberculosis
antigen then they must have current negative chest x-ray to be eligible
- Subject has diarrhea and positive Clostridium difficile (C. difficile) toxin via
stool examination during Screening period. NOTE: Stool examination for C. difficile
toxin will be performed on subjects who have diarrhea during the screening period.
Results of stool tests should be confirmed as negative prior to randomization
We found this trial at
1
site
Click here to add this to my saved trials
