跳至主要内容
临床试验/EUCTR2019-004537-16-FR
EUCTR2019-004537-16-FR进行中(未招募)1 期

Comparison of an inhaled sedation strategy to an intravenous sedation strategy in ICU patients treated with invasive mechanical ventilation - INASED

CHRU de Brest0 个研究点目标入组 250 人开始时间: 2020年9月10日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
250

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Patient aged 18 and over
  • Patient requiring mechanical ventilation for at least 24 hours
  • Consent obtained from the patient or a relative
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patient hospitalized for the following reasons for admission:
  • -Cardiac arrest
  • - State of refractory epilepticus
  • - Head trauma
  • Hearing, visual or aphasia disorders before inclusion
  • Sedation started more than 24 hours ago
  • Impairment of cognitive functions and / or dementia
  • Contraindication to halogenated gases (personal or family history of malignant hyperthermia, acute or chronic neuromuscular disease, hepatocellular insufficiency with PT <30%)
  • Severe SDRA (Berlin criteria)
  • PaCO2 at inclusion> 50 mmHg
  • Pregnancy in progress or lactating woman
  • Patient for whom a procedure of limitation of active therapies is envisaged at inclusion
  • Patient under guardianship or curatorship

研究者

发起方
CHRU de Brest

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