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Trial registered on ANZCTR
Registration number
ACTRN12619000959178
Ethics application status
Approved
Date submitted
5/06/2019
Date registered
8/07/2019
Date last updated
22/12/2021
Date data sharing statement initially provided
8/07/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
Effect of probenecid on the pharmacokinetics of cefalexin in children
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Scientific title
Effect of probenecid on the pharmacokinetics of cefalexin in children
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Secondary ID [1]
298387
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none
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Universal Trial Number (UTN)
U1111-1234-5057
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Trial acronym
CHOC-Dip: Children on cefalexin, dose interval with probenecid
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
antibiotic pharmacokinetics
313073
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Condition category
Condition code
Infection
311560
311560
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0
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Other infectious diseases
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
A single dose of probenecid 10 mg/kg (maximum of 500 mg) orally followed by cefalexin 35 mg/kg (maximum of 1g) orally administered thirty minutes later
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Intervention code [1]
314630
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Treatment: Drugs
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Comparator / control treatment
no control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Total serum cefalexin and probenecid concentrations will be determined using mass spectrometry, Pharmacokinetic parameters to be assessed for each patient are area under the concentration-time curve (AUC) from 0 – 8 h (AUC0-8) and elimination half-life (t1/2)
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Assessment method [1]
320269
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Timepoint [1]
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tests at baseline, 30minutes, 1 hour, 90 minutes, 2 hours, 4 hours, 6 hours and 8 hours
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Secondary outcome [1]
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Side effects (e.g., nausea, rash, headache), allergic reaction measured by direct questioning and direct observation by lead investigator
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Assessment method [1]
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Timepoint [1]
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continously for eight hours
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Eligibility
Key inclusion criteria
Male and female children aged 2-12 years
under the care of the paediatric department at Christchurch hospital
prescribed cefalexin as oral follow-on to iv treatment for osteomyelitis, septic arthritis or other serious infection
have an iv line in place (most likely a PICC line) for blood sampling
receiving no other regular medicines likely to interact with either probenecid or cefalexin
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Minimum age
2
Years
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Maximum age
12
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
children for whom the blood volumes required poses above-minimal risk due to concurrent medical conditions such as anaemia (physician discretion)
contraindication to probenecid eg. hypersensitivity or disorders of uric acid metabolism
contraindication to cefalexin eg. hypersensitivity
taking methotrexate (if treatment is not interrupted while the infection is being treated)
history of significant renal or hepatic disease, or current significant abnormalities in renal or liver function tests.
Children with Cystic Fibrosis
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
open-label, non-randomised, single arm pharmacokinetics study
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Phase
Phase 1
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Type of endpoint/s
Pharmacokinetics
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Statistical methods / analysis
pharmacokinetic data will be analysed using proprietary software
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Recruitment
Recruitment status
Suspended
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Date of first participant enrolment
Anticipated
15/07/2019
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Actual
21/02/2020
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Date of last participant enrolment
Anticipated
1/07/2021
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Actual
21/02/2020
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Date of last data collection
Anticipated
1/08/2021
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Actual
21/02/2020
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Sample size
Target
18
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Accrual to date
1
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Final
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Recruitment outside Australia
Country [1]
21547
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New Zealand
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State/province [1]
21547
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Christchurch
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Funding & Sponsors
Funding source category [1]
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Charities/Societies/Foundations
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Name [1]
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Cure kids
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Address [1]
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c/o Ryan Chandler
PO Box 90 907
Victoria Street
West Auckland 1142
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Country [1]
302928
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New Zealand
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Primary sponsor type
Individual
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Name
A/Prof Tony Walls
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Address
University of Otago
Christchurch School of Medicine
PO Box 4345
Christchurch 8140
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Country
New Zealand
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Secondary sponsor category [1]
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Individual
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Name [1]
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Dr Claire Vivian
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Address [1]
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Department of Child Health
Christchurch Hospital
Riccarton Ave
Christchurch 8140
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Country [1]
302889
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New Zealand
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Other collaborator category [1]
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Individual
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Name [1]
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Professor Steve Chambers, Infectious Diseases Specialist
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Address [1]
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Department of Infectious Diseases
Christchurch Hospital
Private Bag 4710
Christchurch 8140
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Country [1]
280721
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New Zealand
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Other collaborator category [2]
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Individual
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Name [2]
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A/Prof David Reith, Paediatric pharmacologist
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Address [2]
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Office of the Dean
Great King Street
Dunedin School of Medicine
University of Otago 9016
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Country [2]
280722
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New Zealand
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Other collaborator category [3]
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Individual
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Name [3]
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Dr Sharon Gardiner, Antimicrobial pharmacist
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Address [3]
280723
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Dept infectious diseases
Christchurch Hospital, Private Bag 4710
Christchurch 8140
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Country [3]
280723
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New Zealand
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
303492
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NZ Health and Disability Ethics Committee
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Ethics committee address [1]
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Ministry of Health PO Box 5013 Wellington 6145
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Ethics committee country [1]
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New Zealand
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Date submitted for ethics approval [1]
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27/06/2019
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Approval date [1]
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16/10/2019
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Ethics approval number [1]
303492
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NZ Northern A Health and Disability Ethics Committee: 19/NTA/97
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Summary
Brief summary
In adults, probenecid has been shown to approximately double cefalexin concentrations and half-life. To our knowledge, there are no studies investigating the effect of probenecid on the pharmacokinetics of cefalexin in children. Currently cefalexin is given in children as a three times daily dosage. Twice daily dosing would be an advantage over three times daily dosing because it avoids the requirement to consider dosing at school or day care and improves compliance. Co-administration of probenecid with cefalexin may enable this to occur.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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A/Prof Tony Walls
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Address
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University of Otago
Christchurch School of Medicine
PO Box 4345
Christchurch 8140
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Country
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New Zealand
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Phone
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+64 27 262 9968
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Tony Walls
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Address
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University of Otago
Christchurch School of Medicine
PO Box 4345
Christchurch 8140
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Country
93847
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New Zealand
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Phone
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+64 27 262 9968
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Fax
93847
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Email
93847
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[email protected]
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Contact person for scientific queries
Name
93848
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Tony Walls
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Address
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University of Otago
Christchurch School of Medicine
PO Box 4345
Christchurch 8140
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Country
93848
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New Zealand
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Phone
93848
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+64 27 262 9968
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Fax
93848
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Email
93848
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
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What data in particular will be shared?
PK data
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When will data be available (start and end dates)?
Immediately following publication, no end date
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Available to whom?
researchers who provide a methodologically sound proposal and on case-by-case basis at the discretion of Primary Sponsor
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Available for what types of analyses?
meta-analyses and on a case by case basis
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How or where can data be obtained?
access subject to approvals by Principal Investigator
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
14524
Study protocol
[email protected]
14525
Ethical approval
377697-(Uploaded-16-08-2021-09-44-02)-Study-related document.pdf
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF