NL-OMON42622已完成2 期
ociceptive-Level (NoL)-guided analgesia versus standard practice during general remifentanil/propofol anesthesia in ASA 1-3 patients - NoLA
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •1. Age: 18-80 years;
- •2. ASA I-II-III
- •3. Elective open abdominal surgery or laparoscopic assisted abdominal surgery.
排除标准
- •1. Unable to give written informed consent;
- •2. Use of epidural analgesia or local anesthesia (eg. transversus abdominal plain block, TAP block)
- •3. Non-elective surgery
- •4. Pregnancy/lactation;
- •5. BMI > 35 kg/m2;
- •6. Uncontrolled preoperative hypo- or hypertension (Mean arterial pressure < 60 mmHg or > 100 mmHg)
- •7. Preoperative Heart rate < 45/min or > 90/min;
- •8. Central nervous system disorder (neurologic/head trauma/uncontrolled epileptic seizures);
- •9. Illicit substance or alcohol abuse within 30 days;
- •10. Chronic use of pain medication within 30 days;
- •11. Chronic use of psychoactive drugs within 30 days;
- •12. Significant medical condition
- •a. Untreated or persistent peripheral or central cardiovascular disease
- •b. Severe pulmonary disease e.g. COPD gold 4 , FEV< 1.0 L/s, or (evidence of) elevated paCO2 > 6.0 kPa
- •c. Significant hepatic disease with increased bilirubin, INR or low albumin
- •13. Beta blocker use
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