跳至主要内容
临床试验/ISRCTN14587520
ISRCTN14587520已完成未知

The dynamics of the ACTH and cortisol response to CRH stimulation during critical illness: a randomized, double-blind, placebo-controlled crossover study

Katholieke Universiteit Leuven (Belgium)0 个研究点目标入组 60 人开始时间: 2016年7月7日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
60

研究概览

简要总结

2018 Results article in https://www.ncbi.nlm.nih.gov/pubmed/30374692 results

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • For patients:
  • 1. Critically ill patients at the surgical or medical intensive care units, with ongoing intensive care dependency, a stable condition for at least 48h, and an expected stay in ICU for at least 48h
  • 2. Age =18 years
  • For healthy volunteers:
  • 1. Age-, gender- and BMI-matched to the included patients

排除标准

  • For patients:
  • 1. Predisposing factors of adrenal insufficiency
  • 1.1. Cerebral disease with intracranial hypertension threatening the neuroendocrine system
  • 1.2. Pituitary disorders including (pan)hypopituitarism
  • 1.3. Known adrenal disease (Cushing’s syndrome or Addison’s disease)
  • 1.4. Chronic treatment with glucocorticoids, other steroids or anti-steroid chemotherapy within the last 3 months
  • 1.5. IV administration of glucocorticoids within the last 72 hours
  • 1.6. Use of etomidate within the last 72 hours
  • 1.7. Use of azoles within the last 7 days
  • 1.8. Other drugs predisposing to adrenal insufficiency: phenytoin, rifampicin, glitazones, imipramin, phenothiazine, phenobarbital
  • 2. Patients known to be pregnant or nursing
  • 3. No arterial line or central venous catheter in place
  • 4. Ethical restrictions
  • 4.1. Moribund
  • 4.2. Declined participation
  • For healthy volunteers:
  • 1. Recent history of treatment with HPA-axis interfering drugs

研究者

发起方
Katholieke Universiteit Leuven (Belgium)

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