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临床试验/NCT05367531
NCT05367531招募中不适用

Quantitative Assessment of Injectable Medication Delivery Practices

Canadian Forces Health Services Centre Ottawa2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年4月30日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
2
主要终点
Change in medication Injection/delivery time for each trial

研究概览

简要总结

Background:

While medical advances for in-hospital care rapidly evolve, a mainstay of effective pre-hospital care remains the ability to treat medical emergencies such as anaphylaxis, prolonged seizure, overdose, or uncontrolled bleeding, through rapid administration of appropriate medication. Autoinjectors are used globally to deliver medications in a timely manner, often in environments where immediate access to medical facilities is limited. Rapid administration of intramuscular medication delivery is essential where oral or intravenous delivery is either not possible or ineffective. The purpose of the proposed study seeks to determine the efficiency various types of medication injection administration.

详细描述

Research Objective:

To understand the efficiency of injectable medication delivery in the Canadian Forces and civilian world for improved care delivery in military and pre-hospital environments.

Participants:

Approximately thirty (30) participants will be recruited for the study.

Methods:

研究设计

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

盲法说明

The order of administration for each scenario and injection type will be randomized to exclude any bias. To minimize risk to participants, active drug products and live/loaded autoinjectors will not be used. The target injection will be placed in an inanimate object (e.g. orange) or phantom simulator (i.e. inanimate object such as a gel or organic material such as jello or fruit to simulate an injection experience).

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • any participant over the age of 18 able to provide consent

排除标准

  • only participants with pre specified conditions impacting cognitive and/or manual dexterity will be excluded
  • recent substance use
  • non health care workers injection with experience with medication injection in last 12 months

结局指标

主要结局

Change in medication Injection/delivery time for each trial

时间窗: immediately after intervention

Time in seconds will be measured from the start of the scenario and stopped once the medication has been delivered to the orange.

次要结局

  • Number of injection failures and/or injuries associated with each trial(immediately after intervention)
  • Perceived difficulty of injection based on type of system(immediately after intervention)

研究者

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

Gaurav Gupta

Principal Investigator

Canadian Forces Health Services Centre Ottawa

研究点 (2)

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