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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00129688
Other study ID # HE44290
Secondary ID 40/2545
Status Completed
Phase N/A
First received August 10, 2005
Last updated September 22, 2005
Start date April 2002
Est. completion date June 2004

Study information

Verified date February 2005
Source Khon Kaen University
Contact n/a
Is FDA regulated No
Health authority Thailand: Khon Kaen University Ethics Committee for Human Research
Study type Interventional

Clinical Trial Summary

Once-daily dose administration of aminoglycoside in adults is effective and economical. However, its value in febrile neutropenic children, especially in Thailand, is less well researched. In the area where Pseudomonas aeruginosa prevalence in febrile neutropenic children is low, the combination of cloxacillin and amikacin is an appropriate approach. This study would like to compare the efficacy and safety including cost between these two amikacin administrations (once-daily or twice-daily) in combination with cloxacillin as an empirical therapy in febrile neutropenic children.

Hypothesis: Once-daily amikacin plus cloxacillin can be used to treat febrile neutropenic children in Khon Kaen, Thailand.


Description:

Fever: a single oral temperature of >/= 38.3 degrees C; or >/= 38.0 degrees C for >/= 1 hour.

Neutropenia: neutrophil count, < 500/cu mm or <1,000/cu mm with a predicted decrease to <500/mm3.


Recruitment information / eligibility

Status Completed
Enrollment 166
Est. completion date June 2004
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 1 Year to 14 Years
Eligibility Inclusion Criteria:

- Aged 1 year - 14 years

- A single oral temperature of >/= 38.3 degrees C; or >/= 38.0 degrees C for >/= 1 hour.

- Neutropenia: neutrophil count, < 500/cu mm or <1,000/cu mm with a predicted decrease to <500/mm3.

- During the course of chemotherapy

Exclusion Criteria:

- History of amikacin or cloxacillin allergy

- Creatinine clearance < 30 ml/min/m2

- Central nervous system infection: meningitis or brain abscess

- History of hearing abnormality

- Severely ill: shock

- Chronic liver diseases or SGPT > 10 times of upper normal limit

- Received aminoglycoside within 14 days prior to enrolment

- Received any intravenous antibiotics within 7 days

- Cancer which is newly diagnosed or relapsed

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
cloxacillin and amikacin (once or twice daily dosage)


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Khon Kaen University National Research Council of Thailand

Outcome

Type Measure Description Time frame Safety issue
Primary Afebrile within 5 days of the initial treatment regimen
Primary Nephrotoxicity and ototoxicity
Secondary Cost difference
Secondary Pharmacokinetic parameters of amikacin in these children
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