WHO ICTRP trial

USE OF RIFAXIMIN THERAPY IN PRIMARY PREVENTION OF HEPATORENAL SYNDROME IN…

JPRN-UMIN000038487 · Japan Primary Registries Network (JPRN) · Recruiting

Key facts

Trial ID JPRN-UMIN000038487
Public title USE OF RIFAXIMIN THERAPY IN PRIMARY PREVENTION OF HEPATORENAL SYNDROME IN CIRRHOTIC PATIENTS WITH ASCITES
Scientific title USE OF RIFAXIMIN THERAPY IN PRIMARY PREVENTION OF HEPATORENAL SYNDROME IN CIRRHOTIC PATIENTS WITH ASCITES - USE OF RIFAXIMIN THERAPY IN PRIMARY PREVENTION OF HEPATORENAL SYNDROME IN CIRRHOTIC PATIENTS WITH ASCITES
Primary sponsor NationalAcademy of health Sciences,Bir Hospital Department Of Medicine Gastroenterology Unit
Registry Japan Primary Registries Network (JPRN)
Recruitment status Recruiting
Study type Interventional
Phase Not selected
Countries Asia(except Japan)
Conditions Liver Cirrhosis with ascites
Interventions Rifaximin group ,Tab rifaximin at a dose of 550mg BD for 12 weeks and other standard treatment. Non Rifaximin group,Only standar Rx.
Registration date Mar 11, 2019
Target size 94
Registry page center6.umin.ac.jp

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