跳至主要内容
临床试验/EUCTR2015-001110-97-ES
EUCTR2015-001110-97-ES进行中(未招募)1 期

DEXMEDETOMIDINA VERSUS PROPOFOL FOR SEDATION DURING ECOBRONCHOSCOPY - DEXEBUS

Consorci Mar Parc de Salut de Barcelona0 个研究点开始时间: 2015年4月27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)

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

  • Patients under 18 years
  • Patients with suspicion of malignant pulmonary neoplasia who need an ecobronchoscopy under sedation
  • Patients with signed informed consent
  • 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 35
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 35

排除标准

  • Hypersensitivity to the active substance or to any of the included excipients
  • Advanced heart block (grade 2 or 3) unless paced.
  • Uncontrolled hypotension.
  • Acute cerebrovascular conditions.

研究者

相似试验