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临床试验/NCT02563912
NCT02563912已完成不适用

Pre-calculated Doses of Medication for Pediatric Resuscitation, a Simulation Cross-over Randomized Experimental Trial

St. Justine's Hospital2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2015年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
试验地点
2
主要终点
Having at least one dosage error in any of the medications during the case for a participant

研究概览

简要总结

Dosage errors are common in the stressful situation of a pediatric resuscitation. In addition to that, studies have reported that delays to provide medication is associated to worst survival rate for very sick children. To minimize delays and error, the investigators recently published a resuscitation handbook who provides drug dosages for each weight for children thus eliminating the need for dosage calculation. Once the weight of the patient is known, the physicians only have to open the book at the page corresponding to the weight and all the medications with their calculated dosage are provided. The primary goal of this study is to evaluate the number of dosage error during simulated pediatric resuscitation comparing residents using the handbook vs. utilisation of a chart providing non-calculated dosage. This will be an experimental crossover trial among 40 residents performing four simulated case-scenarios in a high-fidelity simulation lab.

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • Residents doing a rotation in pediatrics emergency medicine

排除标准

  • Resident who participated in a previous month

结局指标

主要结局

Having at least one dosage error in any of the medications during the case for a participant

时间窗: During the simulation (10 minutes)

Difference of \> 10% of the recommended drug dosage for any of the medication provided during the simulated case scenario. To be perfect, there must be no error among all drugs provided.

次要结局

  • Time for first drug prescription for each case per participant(During the simulation (10 minutes))
  • Dosage error in any for all individual medications during the case for a participant(During the simulation (10 minutes))

研究者

发起方
St. Justine's Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jocelyn Gravel

MD, MSc, FRCPC

St. Justine's Hospital

研究点 (2)

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