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
| Type | Name | Description |
|---|---|---|
| DRUG | cefepime | Administration 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. |
| DRUG | cefepime | Administration 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.