Efficacy of two different antibiotic prophylactic regimens in liver transplant recipients

Phase 3

Recruiting

• Conditions: liver transplantation.; Liver transplant infection; T86.43

• Registration Number: IRCT20120731010453N2
• Lead Sponsor: Shiraz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 14 January 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 182

Inclusion Criteria

All patients which candidate to liver transplant
older than 18 years old

Exclusion Criteria

Positive history of allergic reactions to antibiotics which use in this study
renal failure patients with hemo-dialysis
serum creatinine levels more than 1.5 mg/dL,blood urea nitrogen (BUN) more than 25 mg/d

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Incidence of bacterial infections in the first month after liver transplantation. Timepoint: During first month after liver transplantation. Method of measurement: Centers for Disease Control and Prevention (CDC) definitions for nosocomial infections.

Secondary Outcome Measures

Name	Time	Method
Mortality rate in liver transplant patients. Timepoint: Duration of hospitalization. Method of measurement: By reviewing patient file information.;Length of intensive care unit stay. Timepoint: Duration of hospitalization. Method of measurement: By reviewing patient file information.;Length of hospital stay. Timepoint: Duration of hospitalization. Method of measurement: By reviewing patient file information.