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Antibiotic Dosing in Pediatric Intensive Care (ADIC)

G

Ghent University Hospital (UZ)

Status

Enrolling

Conditions

Vancomycin
Meropenem
Amikacin
Piperacillin-tazobactam
Ciprofloxacin
Amoxicillin-clavulanate
Teicoplanin
Pharmacokinetics

Treatments

Procedure: blood sampling and urine smapling in patients receiving ciprofloxacin as part of routine clinical care.
Procedure: blood sampling in patients receiving vancomycin as part of routine clinical care.
Procedure: blood sampling in patients receiving teicoplanin as part of routine clinical care.
Procedure: blood sampling in patients receiving amoxicillin-clavulanate as part of routine clinical care
Procedure: blood sampling in patients receiving piperacilline-tazobactam as part of routine clinical care.
Procedure: blood sampling in patients receiving amikacin as part of routine clinical care.
Procedure: blood sampling in patients receiving meropenem as part of routine clinical care.

Study type

Observational

Funder types

Other

Identifiers

NCT02456974
2012/172

Details and patient eligibility

About

Pharmacokinetics of antibiotics in critically ill neonates, infants and children

Enrollment

640 estimated patients

Sex

All

Ages

1 day to 16 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients admitted to the pediatric intensive care unit
  • patient age/weight : 1,8 kg-15 years
  • patient receiving antibiotic treatment (piperacillin-tazobactam, amoxicillin-clavulanate, vancomycin, teicoplanin, meropenem, ciprofloxacin, amikacin) via intermittent infusion regimen or continuous infusion according to institutional treatment guidelines
  • intra-arterial or intravenous access other than the drug infusion line available for blood sampling (arterial line is preferred)

Exclusion criteria

  • no catheter in place for blood sampling
  • absence of parental/patient consent
  • known hypersensitivity to beta-lactam antibiotics, glycopeptides, fluoroquinolones, aminoglycosides
  • extracorporeal circuit (haemodialysis, ECMO, peritoneal dialysis )

Trial design

640 participants in 7 patient groups

amoxicillin-clavulanate
Description:
Patients receiving amoxicillin-clavulanate as part of routine clinical care.
Treatment:
Procedure: blood sampling in patients receiving amoxicillin-clavulanate as part of routine clinical care
piperacilline-tazobactam
Description:
Patients receiving piperacilline-tazobactam as part of routine clinical care.
Treatment:
Procedure: blood sampling in patients receiving piperacilline-tazobactam as part of routine clinical care.
vancomycin
Description:
Patients receiving vancomycin as part of routine clinical care.
Treatment:
Procedure: blood sampling in patients receiving vancomycin as part of routine clinical care.
teicoplanin
Description:
Patients receiving teicoplanin as part of routine clinical care.
Treatment:
Procedure: blood sampling in patients receiving teicoplanin as part of routine clinical care.
meropenem
Description:
Patients receiving meropenem as part of routine clinical care.
Treatment:
Procedure: blood sampling in patients receiving meropenem as part of routine clinical care.
ciprofloxacin
Description:
Patients receiving ciprofloxacin as part of routine clinical care.
Treatment:
Procedure: blood sampling and urine smapling in patients receiving ciprofloxacin as part of routine clinical care.
amikacin
Description:
Patients receiving amikcain as part of routine clinical care.
Treatment:
Procedure: blood sampling in patients receiving amikacin as part of routine clinical care.

Trial contacts and locations

1

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Central trial contact

Pieter De Cock, PharmD

Data sourced from clinicaltrials.gov

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