跳至主要内容
临床试验/NCT04874610
NCT04874610已完成不适用

Steroid Metabolism in Obese and Non-Obese Pediatric Patients Hospitalized for Status Asthmaticus

Duke University1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2021年8月16日最近更新:
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
15
试验地点
1
主要终点
Change in Prednisolone concentration levels as measured by ELISA

研究概览

简要总结

Single center, open-label, non-randomized study to assess the pharmacokinetic profile of methylprednisolone in healthy children 2-20 years of age admitted for asthma exacerbation.

详细描述

This is a prospective study aiming to characterize the pharmacokinetics of methylprednisolone in obese and non-obese children hospitalized for asthma, and to build a metabolomic profile for each cohort. The primary hypothesis is that the obese cohort will have increased methylprednisolone clearance compared to the non-obese cohort. The secondary hypothesis is that the obese cohort will have decreased amounts of 11-β-hydroxysteroid dehydrogenase in the serum which will correlate to abnormalities in steroid clearance. The tertiary hypothesis is that the obese cohort will have increased levels of branched chain amino acids and inflammatory markers which will correlate to disease severity.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
2 Years 至 20 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 2 years and 20 years inclusive
  • Written informed consent provided by a parent or legal guardian
  • Admitted to Duke Children's Hospital for primary reason of asthma exacerbation (and treated with methylprednisolone)
  • BMI-percentile greater than 95th for obese subjects and BMI less than 95th percentile for non-obese subjects

排除标准

  • Patients with suspected liver failure, renal failure, sepsis, or cardiopulmonary instability deemed by the PI.
  • Receiving any extracorporeal life support including extracorporeal membrane oxygenation, ventricular assist devices, and renal replacement therapy at enrollment
  • Any condition or circumstance that, in the opinion of the investigator, would compromise the safety of the participant or the quality of the data.

研究组 & 干预措施

BMI > 95

Cohort 1: greater than or equal to 95%ile body mass index

干预措施: Methylprednisolone (Drug)

BMI < 95

Cohort 2: less than 95%ile body mass index

干预措施: Methylprednisolone (Drug)

结局指标

主要结局

Change in Prednisolone concentration levels as measured by ELISA

时间窗: 0, 24, 48, 72, 96 hours after methylprednisolone dosing

Prednisolone levels at steady state concentration

次要结局

  • 11-beta-hydroxysteroid dehydrogenase as measured by ELISA(Up to 72 hours after methylprednisolone dosing)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验