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临床试验/NCT01973894
NCT01973894已完成不适用

Whole Body Physiologically Based Pharmacokinetic (PBPK) Model to Estimate Cerebral and Systemic Midazolam Concentrations in ICU Patients Under Sedation.

Università degli Studi dell'Insubria1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2013年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20
试验地点
1
主要终点
Midazolam concentration in serum and urine

研究概览

简要总结

This study investigates what independent variables may influence Midazolam Pharmacokinetics in critically ill patients.

详细描述

This study has three specific aims:

  1. to create a Midazolam PBPK model based on anthropometric and physiopathological data from enrolled patients;
  2. to estimate cerebral and systemic Midazolam concentrations;
  3. to assess independent variables about Midazolam pharmacokinetic in critically ill patients.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ICU admittance
  • Caucasian
  • Clinical indication of least 72h of continuous sedation with Midazolam
  • MAP between 60 - 150 mmHg, even if obtained with amine support
  • informed consent obtained

排除标准

  • Any endocranial lesion, spontaneous or induced
  • PaCO2 > 60 mmHg or < 30 mmHg
  • PaO2 < 50 mmHg
  • Pregnancy
  • Any transplantation
  • Severe hepatic failure (Child C)
  • Life expectancy < 72h
  • Ketoconazole and antiretrovirals in therapy

结局指标

主要结局

Midazolam concentration in serum and urine

时间窗: Participants will be followed for the duration of hospital stay, an expected average of 3 weeks

We will calculate Midazolam AUC in serum and urine using blood and urine samples. With this data we will evaluate the elimination constants and create a Physiologically Based Pharmacokinetic Model for Midazolam simulating the drug concentration profile in brain and fat tissue. The blood and urine samples timing is: * 1 blood sample will be gathered after 24h at the beginning of continuous intravenous infusion of Midazolam * 1 blood sample and 1 urine sample will be gathered after 48h at the beginning of continuous intravenous infusion of Midazolam * 1 blood sample will be gathered at the end of continuous intravenous infusion of Midazolam (the duration of infusion is different for each patient according with clinical case) * 1 blood sample and 1 urine sample will be gathered after 6h at the end of continuous intravenous infusion of Midazolam (the duration of infusion is different for each patient according with clinical case)

次要结局

  • Fat mass analysis and its importance in drug distribution.(At enrollment)

研究者

发起方
Università degli Studi dell'Insubria
申办方类型
Other
责任方
Principal Investigator
主要研究者

Paolo Severgnini

Prof.

Università degli Studi dell'Insubria

研究点 (1)

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