Cirrhosis Clinical Trial
Official title:
Fecal Microbial Transplant for Alcohol Misuse in Cirrhosis
There is an epidemic of alcohol use disorder in the US. Alcoholism is an epidemic that spans
all ages and socio-economic strata, which has a major impact on healthcare expenditure.
Alcohol-associated liver disease can take the form of mild fatty liver, chronic liver disease
including cirrhosis and a very acute active form known as alcoholic hepatitis. However, most
patients with alcohol abuse issues with cirrhosis do not develop alcoholic hepatitis and are
not willing to quit drinking. These patients are neither liver transplant candidates due to
their drinking nor have any recourse to therapies directed towards the liver as is the case
with alcoholic hepatitis. This is very large proportion of cirrhotic patients who do not have
many therapeutic options.
Prior studies have demonstrated that these patients have an altered gut-liver axis which is
exacerbated by dysbiosis and a higher production of potentially toxic secondary bile acids.
These secondary bile acids in turn have the potential to worsen the already impaired gut
barrier in these patients, creating a vicious cycle of inflammation and further liver injury
that is led by the altered microbial composition. A gut-based strategy that has the
capability of "resetting" this dysbiosis could help in the amelioration of this inflammatory
load and improve the prognosis of these patients.
Randomized, single-blind, placebo-controlled safety, tolerability study with exploratory
endpoints and pathophysiological evaluation of the FMT
Two groups of outpatients with cirrhosis will be randomized using random sequence generator
into no-treatment and FMT groups.
Once patients are randomized 1:1 into group 1 (FMT) and group 2 (Placebo), both will be
followed over 31 days and will include a 6 month visit to collect samples, perform
questionnaires and to assess SAEs.
There is an epidemic of alcohol use disorder in the US. Alcoholism is an epidemic that spans
all ages and socio-economic strata, which has a major impact on healthcare expenditure.
Alcohol-associated liver disease can take the form of mild fatty liver, chronic liver disease
including cirrhosis and a very acute active form known as alcoholic hepatitis. However, most
patients with alcohol abuse issues with cirrhosis do not develop alcoholic hepatitis and are
not willing to quit drinking. These patients are neither liver transplant candidates due to
their drinking nor have any recourse to therapies directed towards the liver as is the case
with alcoholic hepatitis. This is very large proportion of cirrhotic patients who do not have
many therapeutic options.
Prior studies have demonstrated that these patients have an altered gut-liver axis which is
exacerbated by dysbiosis and a higher production of potentially toxic secondary bile acids.
These secondary bile acids in turn have the potential to worsen the already impaired gut
barrier in these patients, creating a vicious cycle of inflammation and further liver injury
that is led by the altered microbial composition. The investigators believe that a gut-based
strategy that has the capability of "resetting" this dysbiosis can help in the amelioration
of this inflammatory load and improve the prognosis of these patients.
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