Evaluation of Safety & Efficacy of Synbiotic on the Incidence and Recurrence of Spontaneous Bacterial Peritonitis (SBP) in Cirrhotics
Primary Purpose
Cirrhosis With Ascites
Status
Completed
Phase
Phase 3
Locations
India
Study Type
Interventional
Intervention
Norfloxacin + Synbiotic
Norfloxacin + Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Cirrhosis With Ascites
Eligibility Criteria
Inclusion Criteria:
Cirrhosis with ascites with any one of following:
- History of at least one episode of SBP, or
- Ascitic fluid protein less than or equal to 1g/dL, or
- Serum bilirubin more than or equal to 2.5 mg/dL
Exclusion Criteria:
- Renal failure
- HCC
- Hepatic encephalopathy
- No consent
Sites / Locations
- Department of Gastroenterology, G B Pant Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Norfloxacin + Synbiotic
Norfloxacin + Placebo
Arm Description
Outcomes
Primary Outcome Measures
Development of SBP
Secondary Outcome Measures
Mortality
Full Information
NCT ID
NCT00947336
First Posted
July 27, 2009
Last Updated
July 27, 2009
Sponsor
Govind Ballabh Pant Hospital
Collaborators
Jhaver Research Foundation Limited
1. Study Identification
Unique Protocol Identification Number
NCT00947336
Brief Title
Evaluation of Safety & Efficacy of Synbiotic on the Incidence and Recurrence of Spontaneous Bacterial Peritonitis (SBP) in Cirrhotics
Official Title
Evaluation of Safety and Efficacy of Synbiotic on the Incidence and Recurrence of Spontaneous Bacterial Peritonitis in Cirrhotics: A Randomized, Double Blind Placebo Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2009
Overall Recruitment Status
Completed
Study Start Date
April 2005 (undefined)
Primary Completion Date
April 2008 (Actual)
Study Completion Date
April 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Govind Ballabh Pant Hospital
Collaborators
Jhaver Research Foundation Limited
4. Oversight
5. Study Description
Brief Summary
Background: Spontaneous bacterial peritonitis (SBP) is a serious complication in patients of cirrhosis with ascites and may occur despite antibiotic prophylaxis. Small bowel dysmotility and bacterial overgrowth have been documented to be related to SBP. Aims: To investigate whether addition of prebiotic plus probiotics (synbiotics) to norfloxacin enhances the efficacy of norfloxacin in prevention of SBP in high risk patients with ascites.
Methods: A prospective, double blind, randomized controlled trial was conducted in consecutive high-risk cirrhotic patients with ascites who had either recovered from an episode of SBP (secondary prophylaxis) or who never had SBP but were at high risk for development of SBP (low ascitic fluid protein or serum bilirubin ≥2.5 mg/dL; primary prophylaxis). Norfloxacin 400 mg once daily with synbiotic capsules (Streptococcus faecalis JPC 30 million, Clostridium butyricum 2 million, Bacillus mesentericus JPC 1 million, Lactobacillus sporogenes 50 million spores) 2 t.i.d. (group I) or norfloxacin 400 mg once daily with placebo (group II) was given and occurrence of SBP within a period of 6 months (primary endpoint) or side-effects of therapy and mortality (secondary endpoints) were recorded. Every patient received IV albumin to maintain a serum albumin level of >3.2 g/dl. SBP was treated with intravenous antibiotics with albumin.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cirrhosis With Ascites
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
110 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Norfloxacin + Synbiotic
Arm Type
Active Comparator
Arm Title
Norfloxacin + Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Norfloxacin + Synbiotic
Intervention Description
Norfloxacin 400 mg once daily with synbiotic capsules (Streptococcus faecalis JPC 30 million, Clostridium butyricum 2 million, Bacillus mesentericus JPC 1 million, Lactobacillus sporogenes 50 million spores) 2 t.i.d.
Intervention Type
Drug
Intervention Name(s)
Norfloxacin + Placebo
Intervention Description
Norfloxacin 400 mg once daily with placebo
Primary Outcome Measure Information:
Title
Development of SBP
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Mortality
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Cirrhosis with ascites with any one of following:
History of at least one episode of SBP, or
Ascitic fluid protein less than or equal to 1g/dL, or
Serum bilirubin more than or equal to 2.5 mg/dL
Exclusion Criteria:
Renal failure
HCC
Hepatic encephalopathy
No consent
Facility Information:
Facility Name
Department of Gastroenterology, G B Pant Hospital
City
New Delhi
State/Province
Delhi
ZIP/Postal Code
110002
Country
India
12. IPD Sharing Statement
Learn more about this trial
Evaluation of Safety & Efficacy of Synbiotic on the Incidence and Recurrence of Spontaneous Bacterial Peritonitis (SBP) in Cirrhotics
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