EUCTR2022-002892-12-BE进行中(未招募)1 期
Comparison of the efficacy of ephedrine versus norepinephrine in the treatment of hypotension occurring after induction of general anesthesia in patients with chronic renal failure: randomized double-blind pilot study
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
- CHU Brugmann
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Age between 18 and 75 years old
- •Signed informed consent
- •Elective, non-cardiac surgery
- •General anaesthesia
- •Chronic renal failure with a GFR less than 45ml/min/m2 (stages below grade 3b and chronically on dialysis).
- •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 25
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 35
排除标准
- •Congestive heart failure with LVEF < 50%
- •Moderate or severe cardiomyopathy or valvulopathy
- •History of atrial or ventricular arrhythmia
- •Taking drugs from the class of ACE inhibitors and sartans <24 hours before anesthesia
- •Chronic treatment with central antihypertensives such as a2 agonists
- •Chronic treatment with antidepressants of the following classes: selective norepinephrine reuptake inhibitors, tricyclic antidepressants, serotonin and norepinephrine reuptake inhibitors, norepinephrine and dopamine reuptake inhibitors, monoamine oxidase inhibitors.
- •BMI <18.5kg/m2 or >35kg/m2
- •ASA score = 4
- •Pregnant women
- •Allergy to a product used for anesthesia
- •Prone position required during surgery.
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