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To study the efficacy of Rifaximin (drug) vs Norfloxacin (drug) in liver disease

Phase 2
Conditions
Health Condition 1: K769- Liver disease, unspecified
Registration Number
CTRI/2023/12/060803
Lead Sponsor
Institute of Liver and Biliary Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1) Age >18 years

2) Cirrhosis (of any etiology) with ascites

3) Prior incident SBP

Exclusion Criteria

1.Allergy to norfloxacin or rifaximin

2.Recent history of upper gastrointestinal bleed (UGIB) within 2 weeks

3.Patients with a history of multiple episodes of SBP

4.Patients with inoperable or not treatable HCC or other non-hepatic malignancy

5.Patients on immunosuppression

6.HIV infected

7.Post liver transplant

8.Recent ( <6 months) abdominal surgery

9.Pregnant/lactating women

10.Other causes of ascites like tubercular or malignancy

11.Patients developing SBP on Norfloxcacin

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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