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临床试验/NCT02297906
NCT02297906终止1 期

Pharmacokinetics of Intranasal Ketorolac in Children

Columbia University1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2015年2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
终止
入组人数
18
试验地点
1
主要终点
Cmax of intranasal ketorolac

研究概览

简要总结

Ketorolac is a non-steroidal anti-inflammatory drug (NSAID) that is typically given to both adults and children by the intravenous (IV) or intramuscular (IM) route for analgesic purposes. Ketorolac can also be given by the intranasal (IN) route using a mucosal atomization device (MAD). We aim to study the pharmacokinetics of ketorolac when administered by the IN route using the MAD.

详细描述

The intranasal (IN) route of administering medications is an effective means of delivering analgesics to children in a painless and minimally distressing manner, especially in comparison to traditional means of intravenous (IV) or intramuscular (IM) administration, which require a painful and distressing needle stick.

Ketorolac is an analgesic that is commonly administered to children, and can be given by the IN route, in addition to the IV and IM routes. However, the pharmacokinetics of intranasal ketorolac when administered in children has only been described in a limited fashion. The administration of IN ketorolac in children, using the proprietary SPRIX device, which atomizes a fixed amount of ketorolac, produces serum concentrations of ketorolac that are associated with analgesia. However, the concentrations of ketorolac achieved using a mucosal atomization device (MAD) has not yet been evaluated in children presenting to the emergency department. The MAD is a plastic device that attaches to the top of a syringe (see figure). The MAD is much more commonly used for atomizing medications; allows a variable dosage to be administered; and has been shown to be a means of effectively delivering other analgesics and sedatives intranasally.

The purpose of this study is to assess the pharmacokinetics of IN ketorolac when using a MAD to deliver the medication in children presenting to the emergency department. We will determine the maximum serum concentration achieved (Cmax), time to maximum serum concentration achieved (Tmax), and bioavailability (compared to IV ketorolac) when ketorolac is administered intranasally using a MAD.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
8 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Present to the emergency department with a painful condition for which the treating physician decides to administer ketorolac as part of their usual care.

排除标准

  • Known allergy to ketorolac
  • Contraindication to receiving ketorolac
  • Receiving any NSAID within the past 6 hours
  • Presence of an intranasal obstruction that cannot be readily cleared using suction or nose-blowing
  • Inability to speak English or Spanish
  • Critical illness

研究组 & 干预措施

Intranasal ketorolac

Experimental

Ketorolac 0.5 mg/kg, maximum single dose = 30 mg. Administered once by intranasal route using a mucosal atomization device.

干预措施: Ketorolac (Drug)

Intravenous ketorolac

Active Comparator

Ketorolac 0.5 mg/kg, maximum single dose = 30 mg. Administered once by intravenous route.

干预措施: Ketorolac (Drug)

结局指标

主要结局

Cmax of intranasal ketorolac

时间窗: 60 minutes

Maximum serum concentration of ketorolac, after intranasal administration

次要结局

  • Bioavailability of intranasal ketorolac(6 hours)
  • Tmax of intranasal ketorolac(6 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Daniel S Tsze, MD, MPH

Assistant Professor of Pediatrics at CUMC

Columbia University

研究点 (1)

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