Norfloxacin Versus Ciprofloxacin for Spontaneous Bacterial Peritonitis (SBP) Prevention

Korea University

Status and phase: Completed; Phase 4

Conditions: Adverse Reaction to Other Drugs and Medicines

Treatments: Drug: Norfloxacin; Drug: ciprofloxacin

Study type: Interventional

Funder types: Other

Identifiers

NCT01542801

SBP_prevention

Details and patient eligibility

About

• For the prevention of spontaneous bacterial peritonitis (SBP) in patients with liver cirrhosis, norfloxacin 400mg per day is a standard regimen.
• Ciprofloxacin 750 mg per week is also known to be effective for prevention of SBP. In addition, ciprofloxacin once weekly administration is more convenient and less costly.
• Therefore ciprofloxacin once weekly could be more useful if the the efficacy is comparable to norfloxacin once daily.
• This study aims to prove ciprofloxacin once weekly administration is as effective as norfloxacin once daily administration for the prevention of SBP in cirrhotic patients with ascites.

Full description

Spontaneous bacterial peritonitis (SBP) is one of the most serious complication of liver cirrhosis.

The short term mortality reaches 20-30% mainly due to sepsis, hepatorenal syndrome, and liver failure. In addition, patients who suffered SBP show poor prognosis with 1 year-mortality of 50-70%. The high recurrence rate is also problematic. Therefore appropriate prevention of SBP is critically needed to improve survival as well as quality of life.

Selective intestinal decontamination (SID) is eradicating gram negative bacterial in the gut lumen, and effectively prevent development of SBP. Patients with gastrointestinal hemorrhage, low ascitic protein level, high bilirubin, or history of SBP need SID.

Norfloxacin 400 mg daily administration decreased the incidence of SBP to 2% compared with 17% of no prevention group's among patients with ascitic protein less than 1.5 g/dL. Also, in high risk patients (Child-Pugh score > or = 9 points and serum bilirubin level > or = 3 mg/dL, serum creatinine level > or = 1.2 mg/dL, blood urea nitrogen level > or = 25 mg/dL, or serum sodium level < or = 130 mEq/L), norfloxacin 400 mg/day improved 1 year-survival to 60% compared with 48% of no prevention group's. Therefore norfloxacin is now primarily recommend for the prevention of SBP in cirrhotic patients. However, norfloxacin should be administered on daily basis, so efforts to reduce cost and frequency have been made.

Ciprofloxacin 750 mg weekly administration has been evaluated, and shown to be effective as 3.6% versus 22% in prevention versus no prevention arm, respectively. Therefore, ciprofloxacin 750 mg/week is a reasonable option for prevention of SBP. However, comparison of efficacy of these two methods (norfloxacin 400 mg daily versus ciprofloxacin 750 mg weekly) has not been performed, yet.

The investigators aim to compare the efficacy and safety of norfloxacin 400 mg daily and ciprofloxacin 750 mg weekly for the proper management of cirrhotic patients with ascites.

Enrollment: 124 patients

Sex: All

Ages: 20 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age between 20-75 years old
• Liver cirrhosis with ascites
• Ascitic polymorphonucleated cells (PMN) count < 250/mm3
• Ascitic protein <= 1.5 g/dL or History of SBP

Exclusion criteria

• Incompatibility with inclusion criteria
• Hypersensitivity or intolerability with quinolones
• Hepatocellular carcinoma beyond Milan Criteria
• Hepatic encephalopathy over stage 2
• History of treatment with antibiotics within 2 weeks of enrollment
• HIV infection
• Untreated malignancy
• Women with child-bearing age not willing to use effective contraception.
• Pregnant or breast feeding women
• Not able to give informed consents

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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124 participants in 2 patient groups

Norfloxacin

Active Comparator group

Description:

norfloxacin 400 mg once daily administration

Treatment:

Drug: Norfloxacin

Ciprofloxacin

Experimental group

Description:

Ciprofloxacin 750 mg per week

Treatment:

Drug: ciprofloxacin