Overview

Prolonged or Standard Infusion of Cefepime Hydrochloride in Treating Patients With Febrile Neutropenia

Status:
Completed
Trial end date:
2012-10-01
Target enrollment:
0
Participant gender:
All
Summary
This randomized pilot clinical trial studies how well giving prolonged infusion compared to standard infusion of cefepime hydrochloride works in treating patients with febrile neutropenia. Giving cefepime hydrochloride over a longer period of time may be more effective than giving cefepime hydrochloride over the standard time.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Wake Forest University Health Sciences
Collaborator:
National Cancer Institute (NCI)
Treatments:
Cefepime
Cephalosporins
Criteria
Inclusion Criteria:

- Absolute neutrophil count < 500 cells/mm^3 or < 1000 cells/mm^3 with a predicted
decrease to < 500 cells/mm^3

- Temperature > 38.0 degrees Celsius

- Received chemotherapy or stem-cell transplant as treatment for malignancy or
myelodysplastic syndrome (MDS)

- Cefepime prescribed at a dose of 2 grams IV every 8 hours

Exclusion Criteria:

- Allergy to a cephalosporin antibiotic

- Estimated creatinine clearance < 50 milliliters/minute

- Concurrent anti-gram negative antimicrobials

- Diagnostic criteria suggestive of sepsis

- Circumstances which may make 3 hour infusion impractical

- Solid tumor malignancy