Rifaximin for the Secondary Prevention of Spontaneous Bacterial Peritonitis Recurrence in Cirrhotic Patients
Primary Purpose
Spontaneous Bacterial Peritonitis
Status
Withdrawn
Phase
Phase 3
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Rifaximin
Ciprofloxacin
Sponsored by
About this trial
This is an interventional prevention trial for Spontaneous Bacterial Peritonitis focused on measuring liver cirrhosis, ascites, spontaneous bacterial peritonitis, recurrence
Eligibility Criteria
Inclusion Criteria:
- Patients diagnosed with cirrhosis based on clinical, biochemical, ultrasonographic and/or histological criteria
- Patients who had recovered from an episode of spontaneous bacterial peritonitis
- Age > 18 and <80 years
Exclusion Criteria:
Decompensated cirrhotic patients with
- serum bilirubin > 3.2 mg/dL
- prothrombin time < 25%
- serum creatinine > 3 mg/dL
- Active gastrointestinal bleeding
- Hepatic encephalopathy > grade 2
- Patients who have clinical, biochemical or radiological data suggesting hepatocellular carcinoma
Sites / Locations
- Seoul National University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Rifaximin group
Control group
Arm Description
Rifaximin 1200 mg/day orally for 6 months
Ciprofloxacin 500 mg/day orally for 6 months
Outcomes
Primary Outcome Measures
The recurrence rate of spontaneous bacterial peritonitis
The proportion of patients who recurred spontaneous bacterial peritonitis.
Secondary Outcome Measures
mortality
All-cause mortality and cause-specific mortality (mortality due to spontaneous bacterial peritonitis)
The recurrence of culture-negative spontaneous bacterial peritonitis
The proportion of patients who recurred culture-negative spontaneous bacterial peritonitis.
Causative bacteria of recurrent spontaneous bacterial peritonitis
Causative bacteria of recurrent spontaneous bacterial peritonitis and susceptibility
Change of gut microbiota
Gut microbiota will be analyzed at baseline and week 12
Infections other than spontaneous bacterial peritonitis
Infections other than spontaneous bacterial peritonitis (i.e. urinary tract infection, respiratory tract infection, etc.)
Full Information
NCT ID
NCT02011841
First Posted
December 10, 2013
Last Updated
April 24, 2017
Sponsor
Seoul National University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02011841
Brief Title
Rifaximin for the Secondary Prevention of Spontaneous Bacterial Peritonitis Recurrence in Cirrhotic Patients
Official Title
Rifaximin for the Secondary Prevention of Spontaneous Bacterial Peritonitis Recurrence in Cirrhotic Patients: A Prospective, Multicenter, Randomized, Open-label, Controlled Phase III Study
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Withdrawn
Why Stopped
We failed to recruit patients
Study Start Date
January 2014 (undefined)
Primary Completion Date
December 2015 (Anticipated)
Study Completion Date
December 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this study is to evaluate whether long-term rifaximin administration reduces spontaneous bacterial peritonitis recurrence rate in cirrhotic patients.
Detailed Description
Rifaximin is an antibiotic with a broad-spectrum activity against gram-positive and gram-negative microorganisms, both aerobes and anaerobes within the gastrointestinal tract. The main advantage of rifaximin is that it is poorly absorbable, which minimizes the antimicrobial resistance and adverse events and renders the drug safe in all patient populations. In addition, rifaximin has a better activity against gram-positive organisms than norfloxacin.
The appreciation of the potential role of enteric flora in the pathogenesis of several gastrointestinal diseases has broadened the clinical use of rifaximin, which is now used for hepatic encephalopathy, small intestine bacterial overgrowth, inflammatory bowel disease, and Clostridium difficile infection. Theoretically, by reducing the total number of the gut bacteria, rifaximin could also be used to achieve intestinal decontamination in patients with liver cirrhosis and ascites, thus preventing spontaneous bacterial peritonitis.
A small retrospective study concluded that rifaximin suppresses intestinal bacterial overgrowth, bacterial translocation in cirrhotic patients with ascites with no history of previous spontaneous bacterial peritonitis episodes. Prospective clinical trials are warranted to evaluate the role of rifaximin for prevention of spontaneous bacterial peritonitis recurrence in cirrhotic patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spontaneous Bacterial Peritonitis
Keywords
liver cirrhosis, ascites, spontaneous bacterial peritonitis, recurrence
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Rifaximin group
Arm Type
Experimental
Arm Description
Rifaximin 1200 mg/day orally for 6 months
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Ciprofloxacin 500 mg/day orally for 6 months
Intervention Type
Drug
Intervention Name(s)
Rifaximin
Other Intervention Name(s)
Normix
Intervention Description
rifaximin 1200 mg/day orally for 6 months
Intervention Type
Drug
Intervention Name(s)
Ciprofloxacin
Intervention Description
ciprofloxacin 500 mg/day orally for 6 months
Primary Outcome Measure Information:
Title
The recurrence rate of spontaneous bacterial peritonitis
Description
The proportion of patients who recurred spontaneous bacterial peritonitis.
Time Frame
every 4 weeks, up to 24 weeks
Secondary Outcome Measure Information:
Title
mortality
Description
All-cause mortality and cause-specific mortality (mortality due to spontaneous bacterial peritonitis)
Time Frame
up to 24 weeks
Title
The recurrence of culture-negative spontaneous bacterial peritonitis
Description
The proportion of patients who recurred culture-negative spontaneous bacterial peritonitis.
Time Frame
every 4 weeks, up to 24 weeks
Title
Causative bacteria of recurrent spontaneous bacterial peritonitis
Description
Causative bacteria of recurrent spontaneous bacterial peritonitis and susceptibility
Time Frame
every 4 weeks, up to 24 weeks
Title
Change of gut microbiota
Description
Gut microbiota will be analyzed at baseline and week 12
Time Frame
at baseline, week 12
Title
Infections other than spontaneous bacterial peritonitis
Description
Infections other than spontaneous bacterial peritonitis (i.e. urinary tract infection, respiratory tract infection, etc.)
Time Frame
every 4 weeks, up to 24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients diagnosed with cirrhosis based on clinical, biochemical, ultrasonographic and/or histological criteria
Patients who had recovered from an episode of spontaneous bacterial peritonitis
Age > 18 and <80 years
Exclusion Criteria:
Decompensated cirrhotic patients with
serum bilirubin > 3.2 mg/dL
prothrombin time < 25%
serum creatinine > 3 mg/dL
Active gastrointestinal bleeding
Hepatic encephalopathy > grade 2
Patients who have clinical, biochemical or radiological data suggesting hepatocellular carcinoma
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeong-Hoon Lee, M.D., Ph.D.
Organizational Affiliation
Seoul National University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Seoul National University Hospital
City
Seoul
Country
Korea, Republic of
12. IPD Sharing Statement
Learn more about this trial
Rifaximin for the Secondary Prevention of Spontaneous Bacterial Peritonitis Recurrence in Cirrhotic Patients
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