Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | Rifaximin | rifaximin 1200 mg daily versus norfloxacin 400 mg once daily |
| DRUG | Norfloxacin | FDA 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.