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临床试验/NCT01595399
NCT01595399Unknown4 期

Atropine Versus no Atropine for Neonatal Rapid Sequence Intubation

University of Manitoba1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2012年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
70
试验地点
1
主要终点
Heart rate less than 80 BPM and oxygen saturation less than 80%

研究概览

简要总结

The purpose of this study is to compare heart rate in infants who receive atropine as a part of their medication before intubation to those who do not.

To be able to find out , we need to divided babies into 2 groups;

group 1 : receives atropine + sedation + muscle relaxant group 2 : receives water or saline ( placebo group) + sedation + muscle relaxant

Then we need to compare heart rate during intubation and duration of intubation between the 2 groups.

详细描述

We hypothesize that premedication for intubation with fentanyl and succinylcholine alone will maintain equal stability of heart rate and oxygen saturation without a prolongation of time to completion of intubation when compared to a protocol using atropine, fentanyl and succinylcholine.

In order to answer this question we plan to undertake a prospective randomized double blinded control trial of use of atropine as an adjunct for elective intubation of infants less than 46 weeks postmenstrual age.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
1 Day 至 2 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Any infant (preterm and term) up to 46 weeks corrected age requiring (nonemergent) intubation.
  • IV access is obtained
  • Informed parental consent

排除标准

  • Emergent intubation or need for resuscitation
  • Congenital cyanotic heart disease
  • Obvious airway abnormalities
  • History of myopathy or family history of malignant hyperthermia or known history of phosphocholinesterase deficiency

研究组 & 干预措施

Atropine, fentanyl and succinylcholine

Active Comparator

20 mcg/kg atropine IV, 3 mcg/kg fentanyl slowly IV and 2 mg/kg succinylcholine IV.

干预措施: atropine (Drug)

placebo, fentanyl and succinylcholine

Placebo Comparator

an equivalent volume of normal saline to atropine IV, 3 mcg/kg fentanyl slowly IV and 2 mg/kg succinylcholine IV.

干预措施: Placebo (Drug)

结局指标

主要结局

Heart rate less than 80 BPM and oxygen saturation less than 80%

时间窗: 5-6 minutes

Heart rate and transcutaneous oxygen saturation will be monitored continuously during the procedure and data will be recorded at 3 stages; 1. 2 minutes prior to intubation (after atropine or placebo dose) 2. during intubation 3. 2 minutes after intubation (once ETT secured to face)

次要结局

  • Duration of intubation attempts(1-2 minutes)
  • Number of intubation attempts(5-6 minutes)
  • Lowest heart rate after premedication(5-6 minutes)
  • Lowest oxygen saturation after premedication(5-6 minutes)
  • Heart rate < 100 BPM(5-6 minutes)
  • Oxygen saturation < 85%(5-6 minutes)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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