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
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