Clinical Trials Directory

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UnknownNCT02120196

Comparative Study of Rifaximin Versus Norfloxacin in the Secondary Prophylaxis of Spontaneous Bacterial Peritonitis

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Sherief Abd-Elsalam · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The aim of the study is to compare the effectiveness of rifaximin versus norfloxacin for secondary prevention of spontaneous bacterial peritonitis in patients with liver cirrhosis and ascites.

Detailed description

This study will be carried out on 100 patients with liver cirrhosis and ascites who will be enrolled from Tanta University, Tropical Medicine Department in the period between January 2014 to 6 months. The selected patients will be randomly assigned to receive 400 mg of norfloxacin daily or 1200 mg of rifaximin daily and will be classified into two groups : Group 1 : 50 patients will be treated with 1200 mg of rifaximin daily. Group 2 : 50 patients will be treated with 400 mg of norfloxacin daily.

Conditions

Interventions

TypeNameDescription
DRUGRifaximinrifaximin 1200 mg daily versus norfloxacin 400 mg once daily
DRUGNorfloxacinFDA approved:400mg once daily

Timeline

Start date
2014-01-01
Primary completion
2023-12-01
Completion
2023-12-01
First posted
2014-04-22
Last updated
2018-01-09

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT02120196. Inclusion in this directory is not an endorsement.