跳至主要内容
临床试验/EUCTR2014-003713-28-SE
EUCTR2014-003713-28-SE进行中(未招募)不适用

What is the post operative opioid-reducing effect of the beta-receptor-agonist esmolol when administered during laparoscopic gastric by-pass surgery? Comparison between standard anesthesia and anesthesia when remifentanil is replaced with esmolol.

niveritetssjukhuset Örebro0 个研究点开始时间: 2014年9月9日最近更新:
适应症
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

  • 1. 18-65 year of age, male or female planned for laparoscopic gastric by-pass surgery
  • 2. Signed and dated informed consent
  • 3. The volunteer is willing and thought to be able to follow the study protocol
  • 4. BMI > 35kg/m2
  • 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 20
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Severe cardiovascular disease or cardiovascular disease with ongoing treament with beta- and/or alfa-receptor antagonist and/or calcium channel inhibitor
  • 2.Ongoing treatment with opioids
  • 3. ECG with atrio-ventricular block II-III or other severe form of conduction disturbance (e.g. long QT-syndrome)
  • 4. Allergy or sensitivity to remifentanil, fentanyl like opioids, esmolol or other compounds
  • 5. Pregnancy or breast feeding.
  • 6. Participation in a ongoing drug study or, during the last year participated in a drug study where opioid is included or participation in a pharmacological study of any kind the last 30 days or where the monitoring is not yet completed

研究者

发起方
niveritetssjukhuset Örebro

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