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临床试验/NCT02249039
NCT02249039已完成1 期

Intravenous Clonidine for Sedation in Infants and Children Who Are Mechanically Ventilated - Dosing Finding Study

Johns Hopkins University1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2015年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
14
试验地点
1
主要终点
Sedation

研究概览

简要总结

Critically ill infants and children who are mechanically ventilated are often given large doses of opiates and benzodiazepines to provide analgesia-sedation. These drugs significantly cause tolerance and dependence, depresses the drive to breathe, and thus prolongs the need for mechanical ventilation and the associated complications. We propose IV CLON could be used as effectively as DEX.

详细描述

All critically ill mechanically ventilated infants and children receive intravenous analgesic-sedatives which often include opiates and benzodiazepines (BENZO). Undesirable side effects from these drugs include respiratory depression, tolerance and dependence. Alpha 2-adrenergic receptor agonists, dexmedetomidine (DEX) and clonidine (CLON) have excellent sedative-analgesics effects, do not cause respiratory depression and are opiate/BENZO sparing. While both are efficacious in providing sedation, several factors have led to a substantial increase in the use of the newer drug DEX over the more established drug CLON in adults, children and infants. However, studies to guide therapy and dosing for infants and children are lacking. While these infants and children do require less opiate/BENZO therapy and fewer days on mechanical ventilation, they quickly develop tolerance to and have significant withdrawal from DEX. This necessitates protracted weaning of DEX and longer length of stay in the pediatric intensive care unit (PICU) since DEX can only be administered as a continuous intravenous (IV) infusion. CLON, on the other hand, has a longer half-life and has formulations that allow for continuous or intermittent IV and oral administration. Dr. Gauda has an approved IND to use the epidural formulation of CLON intravenously in infants and children. The purpose of this pilot study is to determine the effective IV dosing scheme of CLON that can be safely used as an adjunct to analgesic-sedation management for infants and children in the PICU. It will include a total of 24 infants and children with 4 CLON and DEX exposed in each age stratum: 0-3, 4-6, and 7-12 months. We hypothesize that IV CLON can achieve optimal sedation and reduce the need for opiate/BENZO therapy in critically ill infants and children who would otherwise receive DEX, and thus, reduce the length of stay in the PICU. Data from this study will be used to inform a larger randomized trial and will directly benefit infants and children in Baltimore who are critically ill. Funds are requested to cover the cost of the CLON drug levels and the investigational pharmacy.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
1 Day 至 12 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Infants and children age: 0-12 months
  • Intubated and mechanically ventilated in the JHH PICU
  • Meet criteria for starting dexmedetomidine (per PICU protocol)

排除标准

  • Postoperative from complex congenital heart disease
  • Traumatic Brain Injury
  • Major Chromosomal anomaly (Trisomy 13, 18)
  • Any infant or child who is receiving ECMO therapy
  • If death is considered imminent

研究组 & 干预措施

intermittent IV CLON

Experimental

Mechanically ventilated infants and children receive intravenous intermittentClonidine

干预措施: intermittent IV CLON (Drug)

结局指标

主要结局

Sedation

时间窗: 2-8 weeks

Time spent (hrs) with a State Behavioral Scale \<1 without the concurrent escalation of opiates or sedatives within 24 hrs after starting the CLON or DEX

次要结局

  • Length of stay(2-8 weeks)
  • Frequency of cardiovascular occurrences(2 - 8 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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