Skip to content

Cefotaxime Resistance in Treatment of Spontaneous Bacterial Peritonitis

Cefotaxime Resistance in Treatment of Spontaneous Bacterial Peritonitis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02388035
Enrollment
254
Registered
2015-03-13
Start date
2015-03-31
Completion date
2015-06-30
Last updated
2015-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spontaneous Bacterial Peritonitis

Keywords

profiles changes, microorganisms, cefotaxime, SBP, Egyptian, effective antibiotics

Brief summary

Spontaneous bacterial peritonitis (SBP) is a serious complication in cirrhotic patients, and the changes in the microbiological characteristics reported in the last years are impacting the choice of antibiotic used in the treatment. Cefotaxime has been the most extensively studied antibiotic for this infection. It is considered to be one of the first choice antibiotics because of low toxicity and excellent efficacy. Treatment of SBP by intravenous cefotaxime should be administered for a minimum 5 days. Antibiotic-resistant microorganisms have been increasingly reported especially to cefotaxime and its effect on the clinical outcome in treating SBP.

Interventions

DRUGCefotaxime

Sponsors

Dr Ahmed Ali Elbaz
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* patients with liver cirrhosis and ascites and clinical findings suspicious of ascitic fluid infection

Exclusion criteria

* Patients were excluded if they received antibiotics ten days prior to the hospital admission or there is evidence of secondary bacterial peritonitis, tuberculous peritonitis, malignant ascites or ascites due to other causes e.g. cardiac or renal diseases

Design outcomes

Primary

MeasureTime frame
Organisms detected with their antibiotics sensitivity8 months

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026