Rifaximin for Preventing Progression and Complications in Patients With Decompensated Liver Cirrhosis (RPPCLC)

Rifaximin for Preventing Progression and Complications in Patients With Decompensated Liver Cirrhosis: a Multi-center Randomized Prospective Study

It is still not clear whether rifaximin can prevent the progression of liver cirrhosis, reduce the overall complications and improve the survival in patients with decompensated cirrhosis. This is a multi-center open-labelled randomized prospective study to evaluate the efficacy and safety of rifaximin in preventing the progression and complications in cirrhotic patients, and explore its reasonable dosage and possible mechanism. A total of 150 patients with decompensated liver cirrhosis will be enrolled in the study and randomly divided into three groups (the control group (A), the low-dose rifaximin treatment group (B), and conventional dose rifaximin treatment group (C)) with a ratio of 1:2:2. The patients in group B are given rifaximin with the dose of 600mg/d (600mg, qd) for 24 weeks, and the patients in group C are delivered 1200mg/d (600mg, bid) of rifaximin .During the entire study period, all other therapeutic strategies are kept unchanged in all the groups as long as possible. The proportion of patients with progression of cirrhosis, the incidence of total complications and each complication, survival rate and time, liver function and adverse events will be compared among the three groups. This study might provide a new feasible method with clinical application prospects for preventing the progression and reducing the incidence of liver cirrhosis related complications, improve the prognosis of patients with decompensated liver cirrhosis, and save medical resources.

Study Overview

• Status: Recruiting
• Conditions: Decompensated Cirrhosis
• Intervention / Treatment: Drug: Low-dose of Rifaximin; Drug: Conventional dose of Rifaximin

Detailed Description

Rifaximin has been recommended as a prophylactic drug for hepatic encephalopathy (HE) and spontaneous bacterial peritonitis (SBP), the two major complications of liver cirrhosis. However, it is still not clear whether rifaximin can prevent the progression of liver cirrhosis, reduce the overall complications and improve the survival in patients with decompensated cirrhosis. Additionally, the role of rifaximin in the treatment of liver cirrhosis has not been fully clarified. We designed a multi-center open-labelled randomized prospective study to evaluate the efficacy and safety of rifaximin in preventing the progression and complications in cirrhotic patients, and explore its reasonable dosage and possible mechanism. A total of 150 patients with decompensated liver cirrhosis will be enrolled in the study. They will be randomly divided into three groups (the control group (A), the low-dose rifaximin treatment group (B), and conventional dose rifaximin treatment group (C)) with a ratio of 1:2:2. The patients in group B are given rifaximin with the dose of 600mg/d (600mg, qd) for 24 weeks, and the patients in group C are delivered 1200mg/d (600mg, bid) of rifaximin .During the entire study period, all other therapeutic strategies, such as antiviral agents, non-selective beta-blockers, liver protectants, and diuretics, are kept unchanged in all the groups as long as possible. The proportion of patients with progression of cirrhosis, acute decompensation, acute-on-chronic liver failure (ACLF), decompensation and stable decompensated cirrhosis, the incidence of total complications and each complication, survival rate and time, liver function and adverse events will be compared among the three groups. This study might provide a new feasible method with clinical application prospects for preventing the progression and reducing the incidence of liver cirrhosis related complications, improve the prognosis of patients with decompensated liver cirrhosis, and save medical resources.

• Study Type: Interventional
• Enrollment (Estimated): 150
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Xin Zeng, Dr.; Phone Number: 086018918353309; Email: zengxinmd1978@163.com

Study Locations

• China
  • Shanghai, China, 200120
    • Recruiting
    • Shanghai East Hospital
    • Contact: Wen-Na Li, Dr.; Phone Number: 086018661803012; Email: zengxinmd1978@163.com

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• With a clinical diagnosis of decompensated liver cirrhosis on the basis of typical clinical manifestations, laboratory tests, imaging appearances and/or representative pathology results of liver biopsy. Decompensation of the disease was defined by at least having an episode of severe complications, including ascites, SBP, EGVB and HE.

Exclusion Criteria:

• Episodes of overt HE, EGVB or SBP within 4 weeks before the screening visit
• Uncontrolled severe infection or antibiotic use within 2 weeks before the screening visit
• Hepatitis B virus (HBV) DNA ≥ 500 copy/mL，or receipt of standard antiviral treatment for hepatitis B for less than 12 months
• Receiving antiviral treatment for hepatitis C or receipt of antiviral treatment for hepatitis C within 12 months before the screening visit
• If patients with autoimmune liver disease have been treated with ursodeoxycholic acid, hormone or other immunosuppressants, the dose stability time is less than 6 months
• With history of alcoholism in the last 12 weeks or unwilling to stop alcohol abuse after inclusion (≥ 20 g/day for women or ≥ 30 g/day for men)
• With confirmed or suspected malignancies
• Severe jaundice (serum total bilirubin level ≥ 85 μmol/L)
• Obvious renal dysfunction (serum creatinine ≥ 1.2-fold of upper normal limits)
• Severe electrolyte abnormality (serum sodium level < 125 mmol/L )
• Life-threatening leucocytopenia (white blood cell count < 1 × 10^9/L )
• Poorly controlled hypertension, diabetes mellitus or other severe heart and respiratory diseases (NYHA Ⅲ/Ⅳ, COPD GOLD C)
• With drug abuse, methadone treatment, drug dependence or mental illness
• HIV seropositivity
• Known to be allergic to rifaximin
• Pregnant and lactating women or women who do not rule out pregnancy
• Those who have participated in other drug trials within 12 weeks

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
No Intervention: control group; Group A: Patients in the control group were administered only conventional therapy
Experimental: the low-dose rifaximin treatment group; Group B	Drug: Low-dose of Rifaximin; The patients in group B were given rifaximin with the dose of 600mg/d (600mg, qd) for 24 weeks; Other Names: Low-dose of Xifaxan
Experimental: the conventional dose rifaximin treatment group; Group C	Drug: Conventional dose of Rifaximin; the patients in group C were delivered 1200mg/d (600mg, bid) for 24 weeks; Other Names: Conventional dose of Xifaxan

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
The proportion of patients with progression of liver cirrhosis	The proportion of patients with progression of liver cirrhosis, which is defined as at least one additional stage of liver cirrhosis staging during the 24-week treatment phase	24 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Incidence of overall complications resulting from decompensated liver cirrhosis	The incidence of overall complications resulting from decompensated liver cirrhosis in 12weeks and 24weeks, including refractory ascites, SBP, esophageal and gastric variceal bleeding (EGVB), overt hepatic encephalopathy(OHE), cute renal injury (AKI)/hepatorenal syndrome (HRS), primary hepatic carcinoma (PHC), etc.	12 and 24weeks
Incidence of various complications of liver cirrhosis, including: refractory ascites, SBP, EGVB, OHE, AKI/HRS, PHC, etc.	The incidence of each complication resulting from decompensated liver cirrhosis in 12weeks and 24weeks, including refractory ascites, SBP, EGVB, OHE, AKI/HRS, PHC, etc.	12 weeks and 24 weeks
The proportion of patients with progression of liver cirrhosis	The proportion of patients with progression of liver cirrhosis, which is defined as at least one additional stage of liver cirrhosis staging during the 12-week treatment phase	12 weeks
The proportion of patients with acute decompensated (AD)	The proportion of patients with acute decompensated (AD)	12 and 24 weeks
The proportion of patients with stable decompensated cirrhosis	The proportion of patients with stable decompensated cirrhosis, which is defined as patients with decompensated cirrhosis who, while receiving sustained prophylaxis with diuretics, and/or lactulose or rifaximin, and/or non-selective beta-blockers or repeated endoscopic treatment of esophagogastric varices, do not present episodes of AD for a long-time period.	24 weeks
The proportion of patients with recompensation of cirrhosis	The proportion of patients with recompensation of cirrhosis, which is defined as the clinical phase of the disease prior to the resolution of cirrhosis induced by successful treatment of the underlying aetiology.	24 weeks
All-cause mortality	All-cause mortality during the 24-week treatment phase	24 weeks
Complication-free survival time	Complication-free survival time during the treatment phase	24 weeks
Liver transplantation free survival time	Liver transplantation free survival time during the treatment phase	24 weeks
Child-Pugh score	Liver function reflected by Child-Pugh score. A higher Child-Pugh score mean a worse outcome	24 weeks
The proportion of patients with different Child-Pugh class	The proportion of patients with Child-Pugh A/B/C （Child-Pugh A: Child-Pugh score<7; Child-Pugh B: Child-Pugh score 7~9; Child-Pugh C: Child-Pugh score>9 ）	24 weeks
Model for end-stage liver disease (MELD) score	Liver function reflected by MELD score. A higher MELD score mean a worse outcome	24 weeks

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Incidence of ACLF	The proportion of patients with ACLF during the treatment phase	24 weeks
Health-related quality of life (HRQoL)	HRQoL evaluated with chronic liver disease questionnaire,CLDQ)	24 weeks
Sarcopenia	Sarcopenia evaluated with L3 skeletal muscle index (L3-SMI) based on CT or MRI	24 weeks
Myosteatosis	Myosteatosis evaluated with L3 skeletal muscle density (L3-SMD) based on CT or MRI	24 weeks

Collaborators and Investigators

• Sponsor: Xin Zeng
• Investigators: Principal Investigator: Xin Zeng, Dr., Department of Gastroenterology, Shanghai East Hospital, Tongji University School of Medicine

Study record dates

Study Major Dates

• Study Start (Estimated): August 18, 2023
• Primary Completion (Estimated): December 31, 2025
• Study Completion (Estimated): December 31, 2025

Study Registration Dates

• First Submitted: December 28, 2022
• First Submitted That Met QC Criteria: May 16, 2023
• First Posted (Actual): May 18, 2023

Study Record Updates

• Last Update Posted (Actual): August 8, 2023
• Last Update Submitted That Met QC Criteria: August 5, 2023
• Last Verified: May 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Digestive System Diseases; Pathologic Processes; Liver Diseases; Fibrosis; Liver Cirrhosis; Anti-Infective Agents; Gastrointestinal Agents; Anti-Bacterial Agents; Rifaximin
• Other Study ID Numbers: DFYY2022096

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No