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Norfloxacin Versus Ciprofloxacin for Spontaneous Bacterial Peritonitis (SBP) Prevention

Primary Purpose

Adverse Reaction to Other Drugs and Medicines

Status
Completed
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Norfloxacin
ciprofloxacin
Sponsored by
Korea University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Adverse Reaction to Other Drugs and Medicines focused on measuring Effect of Preventive Antibiotics

Eligibility Criteria

20 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept 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

Sites / Locations

  • Korea University Ansan Hospital
  • Soonchunhyang University College of Medicine, Bucheon Hospital
  • Soonchunhyang University College of Medicine, Cheonan Hospital
  • Kyungpuk National University Hospital
  • Korea University Anam Hospital
  • Soonchunhyang University College of Medicine, Seoul Hospital
  • Sungkyunkwan University Gangbuk Samsung Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Norfloxacin

Ciprofloxacin

Arm Description

norfloxacin 400 mg once daily administration

Ciprofloxacin 750 mg per week

Outcomes

Primary Outcome Measures

The prevention rate of spontaneous bacterial peritonitis (SBP)
The incidence of SBP will measured in each the group. Thereby, prevention rate will also be compared between the groups.

Secondary Outcome Measures

1 year mortality
liver related mortality and overall mortality will be assessed.
Incidence of infectious event other than SBP
Bacteremia, urinary tract infection, pneumonia, and other infections will be included.
Hepatorenal syndrome
Diagnostic criteria of hepatorenal syndrome is defined by the latest version of Internation ascites club consensus.
Hepatic encephalopathy
Will follow the Western Heaven Criteria.
Adverse event of drugs
Any of adverse event suspected by study drugs will be recorded.

Full Information

First Posted
February 26, 2012
Last Updated
December 27, 2016
Sponsor
Korea University
Collaborators
Sungkyunkwan University, Kyungpook National University Hospital, Soon Chun Hyang University
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1. Study Identification

Unique Protocol Identification Number
NCT01542801
Brief Title
Norfloxacin Versus Ciprofloxacin for Spontaneous Bacterial Peritonitis (SBP) Prevention
Official Title
Comparison of Daily Norfloxacin Versus Weekly Ciprofloxacin for the Prevention of Spontaneous Bacterial Peritonitis in Cirrhotic Patients
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Completed
Study Start Date
August 2011 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
April 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Korea University
Collaborators
Sungkyunkwan University, Kyungpook National University Hospital, Soon Chun Hyang University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adverse Reaction to Other Drugs and Medicines
Keywords
Effect of Preventive Antibiotics

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
124 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Norfloxacin
Arm Type
Active Comparator
Arm Description
norfloxacin 400 mg once daily administration
Arm Title
Ciprofloxacin
Arm Type
Experimental
Arm Description
Ciprofloxacin 750 mg per week
Intervention Type
Drug
Intervention Name(s)
Norfloxacin
Intervention Description
Norfloxacin 400 mg per day
Intervention Type
Drug
Intervention Name(s)
ciprofloxacin
Intervention Description
Ciprofloxacin 750 mg per week
Primary Outcome Measure Information:
Title
The prevention rate of spontaneous bacterial peritonitis (SBP)
Description
The incidence of SBP will measured in each the group. Thereby, prevention rate will also be compared between the groups.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
1 year mortality
Description
liver related mortality and overall mortality will be assessed.
Time Frame
12 months ( 1 year)
Title
Incidence of infectious event other than SBP
Description
Bacteremia, urinary tract infection, pneumonia, and other infections will be included.
Time Frame
12 months
Title
Hepatorenal syndrome
Description
Diagnostic criteria of hepatorenal syndrome is defined by the latest version of Internation ascites club consensus.
Time Frame
12 months
Title
Hepatic encephalopathy
Description
Will follow the Western Heaven Criteria.
Time Frame
12 months
Title
Adverse event of drugs
Description
Any of adverse event suspected by study drugs will be recorded.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Soon Ho Um, M.D., Ph.D.
Organizational Affiliation
Korea University Anam Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hyung Joon Yim, M.D., Ph.D.
Organizational Affiliation
Korea University Ansan Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Korea University Ansan Hospital
City
Ansan
State/Province
Gyeonggi-do
Country
Korea, Republic of
Facility Name
Soonchunhyang University College of Medicine, Bucheon Hospital
City
Bucheon
Country
Korea, Republic of
Facility Name
Soonchunhyang University College of Medicine, Cheonan Hospital
City
Cheonan
Country
Korea, Republic of
Facility Name
Kyungpuk National University Hospital
City
Daegu
Country
Korea, Republic of
Facility Name
Korea University Anam Hospital
City
Seoul
Country
Korea, Republic of
Facility Name
Soonchunhyang University College of Medicine, Seoul Hospital
City
Seoul
Country
Korea, Republic of
Facility Name
Sungkyunkwan University Gangbuk Samsung Hospital
City
Seoul
Country
Korea, Republic of

12. IPD Sharing Statement

Citations:
PubMed Identifier
11736714
Citation
Mowat C, Stanley AJ. Review article: spontaneous bacterial peritonitis--diagnosis, treatment and prevention. Aliment Pharmacol Ther. 2001 Dec;15(12):1851-9. doi: 10.1046/j.1365-2036.2001.01116.x.
Results Reference
background
PubMed Identifier
17551068
Citation
Koulaouzidis A, Bhat S, Karagiannidis A, Tan WC, Linaker BD. Spontaneous bacterial peritonitis. Postgrad Med J. 2007 Jun;83(980):379-83. doi: 10.1136/pgmj.2006.056168.
Results Reference
background
PubMed Identifier
11786970
Citation
Fernandez J, Navasa M, Gomez J, Colmenero J, Vila J, Arroyo V, Rodes J. Bacterial infections in cirrhosis: epidemiological changes with invasive procedures and norfloxacin prophylaxis. Hepatology. 2002 Jan;35(1):140-8. doi: 10.1053/jhep.2002.30082.
Results Reference
background
PubMed Identifier
20633946
Citation
European Association for the Study of the Liver. EASL clinical practice guidelines on the management of ascites, spontaneous bacterial peritonitis, and hepatorenal syndrome in cirrhosis. J Hepatol. 2010 Sep;53(3):397-417. doi: 10.1016/j.jhep.2010.05.004. Epub 2010 Jun 1. No abstract available.
Results Reference
background
PubMed Identifier
7557868
Citation
Rolachon A, Cordier L, Bacq Y, Nousbaum JB, Franza A, Paris JC, Fratte S, Bohn B, Kitmacher P, Stahl JP, et al. Ciprofloxacin and long-term prevention of spontaneous bacterial peritonitis: results of a prospective controlled trial. Hepatology. 1995 Oct;22(4 Pt 1):1171-4. doi: 10.1016/0270-9139(95)90626-6.
Results Reference
result
PubMed Identifier
9764990
Citation
Grange JD, Roulot D, Pelletier G, Pariente EA, Denis J, Ink O, Blanc P, Richardet JP, Vinel JP, Delisle F, Fischer D, Flahault A, Amiot X. Norfloxacin primary prophylaxis of bacterial infections in cirrhotic patients with ascites: a double-blind randomized trial. J Hepatol. 1998 Sep;29(3):430-6. doi: 10.1016/s0168-8278(98)80061-5.
Results Reference
result
PubMed Identifier
17854593
Citation
Fernandez J, Navasa M, Planas R, Montoliu S, Monfort D, Soriano G, Vila C, Pardo A, Quintero E, Vargas V, Such J, Gines P, Arroyo V. Primary prophylaxis of spontaneous bacterial peritonitis delays hepatorenal syndrome and improves survival in cirrhosis. Gastroenterology. 2007 Sep;133(3):818-24. doi: 10.1053/j.gastro.2007.06.065. Epub 2007 Jul 3.
Results Reference
result
Links:
URL
http://www.korea.ac.kr
Description
Korea University (PI of SBP_prevention study is belong to this university)

Learn more about this trial

Norfloxacin Versus Ciprofloxacin for Spontaneous Bacterial Peritonitis (SBP) Prevention

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