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临床试验/CTRI/2024/11/077222
CTRI/2024/11/077222尚未招募不适用

Effect of use of single dose of Etomidate on serum cortisol levels in patients requiring rapid sequence intubation in ED (ETOCORT trial):An Observational Study

AIG Hospitals1 个研究点 分布在 1 个国家目标入组 47 人开始时间: 2024年12月3日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
AIG Hospitals
入组人数
47
试验地点
1
主要终点
To measure and assess the decrease in serum cortisol levels compared to pre-intubation baseline at 30 minutes and 24 hours post intubation

研究概览

简要总结

Rapid sequence intubation is a critical and time sensitive procedure performed in emergency departments. It involves administration of an induction agent and a paralytic agent to facilitate rapid tracheal intubation. Etomidate is frequently chosen due to its rapid onset and short duration and minimal cardiovascular effects. But it also inhibits cortisol synthesis thereby reducing the cortisol’s levels. Cortisol plays a pivotal role in body’s stress response thereby maintaining blood pressure, metabolism and immune function. The above effect of etomidate led to a growing body of literature examining the clinical implications of its use, particularly in those patients who are susceptible to adrenal insufficiency, for example, sepsis, burns and polytrauma.

This study, therefore aims to investigate the effect of a single dose of Etomidate on cortisol levels in patients undergoing rapid sequence intubation in the ED and thereby evaluating the extent of cortisol suppression and its actual clinical implications

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • Patients receiving a single dose of etomidate as the induction agent for intubation -Patients who can provide informed consent or for whom consent can be obtained from a legally authorized representative.

排除标准

  • Patients with known adrenal insufficiency or receiving chronic corticosteroid therapy.
  • Patients with a recent history of etomidate exposure (Within 24 hours).
  • Patients with contraindications to Etomidate.
  • Pregnant patients.

结局指标

主要结局

To measure and assess the decrease in serum cortisol levels compared to pre-intubation baseline at 30 minutes and 24 hours post intubation

时间窗: 0 minutes, 30 minutes and 24 hours

次要结局

  • all cause mortality(48 hours)

研究者

发起方
AIG Hospitals
申办方类型
Private hospital/clinic
责任方
Principal Investigator
主要研究者

Dr Sarat Chandra Uppaluri

AIG Hospitals

研究点 (1)

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