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临床试验/NCT00491426
NCT00491426已完成不适用

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

Duke University6 个研究点 分布在 1 个国家目标入组 450 人开始时间: 2006年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
450
试验地点
6

研究概览

简要总结

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.

详细描述

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

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

研究设计

研究类型
Observational
时间视角
Retrospective

入排标准

年龄范围
— 至 120 Days(Child)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • Failure to consent

研究组 & 干预措施

26-29 weeks

Subjects 26-29 weeks gestational age

干预措施: Metronidazole (Drug)

<26 weeks

Subjects <26 weeks gestational age

干预措施: Ampicillin (Drug)

<26 weeks

Subjects <26 weeks gestational age

干预措施: Metronidazole (Drug)

<26 weeks

Subjects <26 weeks gestational age

干预措施: Piperacillin/Tazobactam (Drug)

<26 weeks

Subjects <26 weeks gestational age

干预措施: Acyclovir (Drug)

<26 weeks

Subjects <26 weeks gestational age

干预措施: Amphotericin B (Drug)

<26 weeks

Subjects <26 weeks gestational age

干预措施: Ambisome (Drug)

<26 weeks

Subjects <26 weeks gestational age

干预措施: Anidulafungin (Drug)

<26 weeks

Subjects <26 weeks gestational age

干预措施: Caspofungin (Drug)

26-29 weeks

Subjects 26-29 weeks gestational age

干预措施: Ampicillin (Drug)

26-29 weeks

Subjects 26-29 weeks gestational age

干预措施: Piperacillin/Tazobactam (Drug)

26-29 weeks

Subjects 26-29 weeks gestational age

干预措施: Acyclovir (Drug)

26-29 weeks

Subjects 26-29 weeks gestational age

干预措施: Amphotericin B (Drug)

26-29 weeks

Subjects 26-29 weeks gestational age

干预措施: Ambisome (Drug)

26-29 weeks

Subjects 26-29 weeks gestational age

干预措施: Anidulafungin (Drug)

26-29 weeks

Subjects 26-29 weeks gestational age

干预措施: Caspofungin (Drug)

30-32 weeks

Subjects 30-32 weeks gestational age

干预措施: Ampicillin (Drug)

30-32 weeks

Subjects 30-32 weeks gestational age

干预措施: Metronidazole (Drug)

30-32 weeks

Subjects 30-32 weeks gestational age

干预措施: Piperacillin/Tazobactam (Drug)

30-32 weeks

Subjects 30-32 weeks gestational age

干预措施: Acyclovir (Drug)

30-32 weeks

Subjects 30-32 weeks gestational age

干预措施: Amphotericin B (Drug)

30-32 weeks

Subjects 30-32 weeks gestational age

干预措施: Ambisome (Drug)

30-32 weeks

Subjects 30-32 weeks gestational age

干预措施: Anidulafungin (Drug)

30-32 weeks

Subjects 30-32 weeks gestational age

干预措施: Caspofungin (Drug)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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