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临床试验/EUCTR2012-002834-36-NL
EUCTR2012-002834-36-NL进行中(未招募)不适用

Evaluation of the effects of the addition of atropine during propofol/remifentanil induction of anesthesia on hemodynamics, microvascular blood flow and tissue oxygenenation in patients undergoing ophthalmic surgery

MCG0 个研究点开始时间: 2012年6月29日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

  • All patients scheduled to undergo elective ophthalmic surgery under general anesthesia.
  • Patients must be 18 years or older.
  • No selection will be made regarding gender, age, ASA-classification, co-morbidity or ethnic background.
  • 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 60
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range 0

排除标准

  • - Patient’s refusal
  • - Patient’s age < 18 years
  • - Patients in which atropine is contra-indicated, such as severe aortic valve stenosis, hypertrophic cardiomyopathy or coronary artery disease

研究者

发起方
MCG

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Atropine-effect during propofol/remifentanil inductio | 临床试验