Clinical Trials Directory

Trials / Completed

CompletedNCT00609375

Efficacy of Cefepime Continuous Infusion Versus an Intermittent Dosing Regimen

Efficacy of Cefepime Continuous Infusion Versus an Intermittent Dosing Regimen in Adult Critically Ill Patients With Gram Negative Bacilli Bacteremia

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Javeriana University · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

To determine the efficacy of the administration of 7 to 14 days of cefepime in a continuous infusion vs an intermittent (every 8 hours) administration, in adult patients hospitalized in Bogotá with sepsis and bacteremia caused by gram negative bacilli. The outcome was the rate of clinical cure and microbiological cure after 7 and 14 days of initiation of therapy and rates of relapse after 28 days. Hypothesis: The administration of beta lactams in continuous infusion allows a clinical or microbiological cure greater than the intermittent administration.

Conditions

Interventions

TypeNameDescription
DRUGcefepimeAdministration of cefepime in continuous infusion (3 Gr over 24 hours) for 7-14 days at the discretion of the investigator. Administration of saline solution 0.9%, 50-100 mL over 30 minutes every 8 hours.
DRUGcefepimeAdministration of cefepime in intermittent infusion (1 Gr over 30 minutes every 8 hours) for 7-14 days at the discretion of the investigator.Administration of saline solution 0.9%, 50-250 mL over 24 hours

Timeline

Start date
2006-09-01
Primary completion
2007-12-01
Completion
2007-12-01
First posted
2008-02-07
Last updated
2008-02-07

Locations

7 sites across 1 country: Colombia

Source: ClinicalTrials.gov record NCT00609375. Inclusion in this directory is not an endorsement.