Skip to main content
OpenTrials
Completed

NCT Number: NCT00491426

Antimicrobial PK in Infants With Suspected or Confirmed Infection

The purpose of this protocol is to provide a mechanism for the ongoing collection of blood and urine samples in newborns that will be used to measure levels of antimicrobial products used in the newborn population where there are limited pharmacokinetic data in either premature or term infants.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

Up to 120 day

Sex eligibility

All sexes

Study type

Observational

Primary location

University of California at San Diego, La Jolla, California, United States

Loading trial locations.

About this study

Greater than 90% of infants born <32 weeks admitted to critical care nurseries are treated with antimicrobial agents during their NICU hospitalization. Most antimicrobial products used in the neonatal population lack some aspect of pharmacokinetic information specific to neonates. Dosing is based largely on pharmacokinetic data from older children or in some cases, adults. This study will also establish a bank of urine samples from newborns treated with antimicrobial and/or antifungal therapy and to characterize the urinary proteome in selected samples. The sites of the NIH-sponsored Pediatric Pharmacology Research Network (PPRU) have access to appropriate assays using microliter amounts of serum and a large pool of potential subjects to generate meaningful data that will

  • Guide dosing of commonly used antimicrobial agents, and
  • Provide preliminary data for future industry and government trials in the nursery.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Infants ≤32 weeks and 6 days EGA with high probability of receiving one of the antimicrobial agents listed are eligible for study.
  • Age younger than 120 days
  • Written informed consent from parent or legal guardian
  • Infants likely to survive beyond 48 hours after enrollment

Exclusion criteria

  • Failure to consent

Treatment and study plan

Ampicillin

Drug

Drug prescribed per routine medical care.

Metronidazole

Drug

Drug prescribed per routine medical care.

Piperacillin/tazobactam

Drug

Drug prescribed per routine medical care.

Acyclovir

Drug

Drug prescribed per routine medical care.

Amphotericin B

Drug

Drug prescribed per routine medical care.

AmBisome

Drug

Drug prescribed per routine medical care.

Anidulafungin

Drug

Drug prescribed per routine medical care.

Caspofungin

Drug

Drug prescribed per routine medical care.

Sponsors and collaborators

Lead sponsor

Duke University

Other

Collaborators

  • Pediatric Pharmacology Research Units Network

Registry information

Official study title

Antimicrobial Pharmacokinetics in High Risk Infants (Urinary Proteomics in Antimicrobial/Antifungal-Treated Newborns - add-on Study)

Important dates

Study start
2006
Primary completion
2010
Study completion
2010
First posted
Jun 26, 2007
Registry last updated
Nov 19, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.