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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
Govind Ballabh Pant Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cirrhosis With Ascites

Eligibility Criteria

12 Years - 75 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
July 27, 2009
Last Updated
July 27, 2009
Sponsor
Govind Ballabh Pant Hospital
Collaborators
Jhaver Research Foundation Limited
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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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