Efficacy of Rifaximin vs Norfloxacin for Secondary Prophylaxis of SBP (NORRIF Trial)

Spontaneous Bacterial Peritonitis Clinical Trial

Official title:

Efficacy of Rifaximin vs Norfloxacin for Secondary Prophylaxis of SBP (NORRIF Trial): a Randomized Control Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06199843
• Other study ID #: ILBS-SBP-03
• Status: Not yet recruiting
• Phase: N/A
• Start date: January 5, 2024
• Est. completion date: December 31, 2024

Study information

• Verified date: November 2023
• Source: Institute of Liver and Biliary Sciences, India
• Contact: Dr Jayashree Biswas, MD
• Phone: 01146300000
• Email: jayashreeb790[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

SBP is a common complication of cirrhotics with associated increased mortality. After first episode of SBP there is increased risk of again developing SBP, with increased chance of developing resistant organism. So after the first episode of SBP, prophylaxis for prevention of second episode onwards is mandatory and therefore Rifaximin or Norfloxacin is considered. It has been seen that apart from preventing SBP they have other benefits with negligible side effects and therefore it is to be seen what other benefits including mortality benefits these drugs can confer.

Description:

Hypothesis:-Rifaximin will be more effective in decreasing the incidence of SBP in patients with cirrhosis and prior episode of SBP AIM:-.To study the efficacy and safety of Rifaximin vs Norfloxacin in preventing incident SBP, preventing non-SBP infections, and improving transplant free survival in patients with cirrhosis and previous episode of SBP Methodology Single centered Open labeled Randomized Controlled Trial Randomization will be done by block randomization method taking block size as 10. Data will be entered in Microsoft Excel and will be analysed by SPSS Version 28.Categorical Data will be represented as frequency (%) and will be analysed using Chi square or Fisher Exact Test as appropriate.Continuous Data will be represented as Mean +/- SD and compared using Student T test or Mann Whitney as per normality conditions are met or not.Beside this an appropriate analysis like survival analysis will be carried out at the time of Data Analysis.P value <0.05 will be considered as significant. Rescue therapy: To be given to patients who develop SBP while on secondary prophylaxis, these patients will initially be treated by iv medication in hospital settings followed by change in therapy. - Patients in Rifaximin limb developing SBP will switch to Norfloxacin - Patients in Norfloxacin limb developing SBP will switch to Rifaximin Treatment Failure: Defined as development of SBP at end of 6 months or 1 year of treatment. Study population: age >18 years with prior incident SBP Study design: Randomised case controlled trial Study period: 1year after ethical clearance Sample size: 280 (140 in each arm) Intervention: This RCT will be conducted at ILBS New Delhi Monitoring and assessment: Monitoring will be done forall the parameters of the objective. Documentation will be done for any adverse effects which will happen. STATISTICAL ANALYSIS: Assuming incidence of SBP over 6 months is 4% in Rifaximin & 15% in Norfloxacin Alpha 5% and power 80%. Enrollment of 260 cases (130 in each arm). Assuming dropout rate 10%.Total study cases calculated as 280 (140 in each arm). Random allocation in each arm by block method taking 10 as block size

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 280
• Est. completion date: December 31, 2024
• Est. primary completion date: December 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Peritonitis
• Spontaneous Bacterial Peritonitis

Intervention

Drug:
• Rifaximin
Rifaximin 550 mg BD
• Norfloxacin
Norfloxacin 400 mg OD

Locations

Country	Name	City	State
India	Dr Jaya Benjamin	New Delhi	Delhi

Sponsors (1)

Lead Sponsor	Collaborator
Institute of Liver and Biliary Sciences, India

Country where clinical trial is conducted

India, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of recurrence of SBP within 6 months		6 months
Secondary	Incidence of recurrence of SBP within12 months		12 months
Secondary	Incidence of other site infections within 6 months		6 months
Secondary	Incidence of other site infections within 12 months		12 months
Secondary	to look for resistance pattern of infection in both norfloxacin and rifampicin group, type of resistant bacteria (MDR/XDR), and response of both groups to rifampicin and norfloxacin in secondary prophylaxis of SBP		12 months
Secondary	Incidence of other complications (HE, variceal bleed, Refractory ascites, AKI) within 6 months		6 months
Secondary	Incidence of other complications (HE, variceal bleed, Refractory ascites, AKI) within 12 months)		12 months
Secondary	Transplant free survival by 6 months		6 months
Secondary	Transplant free survival by 12 months		12 months
Secondary	Change in Child-Turcotte-Pugh (CTP) by 6 months		6 months
Secondary	Change in Model for End-Stage Liver Disease (MELD) scores by 6 months		6 months
Secondary	Change in Model for End-Stage Liver Disease Sodium (MELD Na) scores by 6 months		6 months
Secondary	Change in Child-Turcotte-Pugh (CTP) scores by 12 months		12 months
Secondary	Change in Model for End-Stage Liver Disease (MELD) scores by 12 months		12 months
Secondary	Change in MELD-Na scores by 12 months		12 months
Secondary	Side effects in both groups		12 months