跳至主要内容
临床试验/NL-OMON48484
NL-OMON48484已完成不适用

Sevoflurane/fentanyl anesthesia guided by Nociceptive-Level index during abdominal surgery in ASA 1-3 patients * a randomized controlled trial on the effect of NOL-guidance on postoperative pain scores - SOLAR

eids Universitair Medisch Centrum0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20

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

年龄范围
18 至 99(—)

入选标准

  • 1. Age: 18 years and older;
  • 2. ASA I-II-III
  • 3. Elective 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.
  • 6. Uncontrolled preoperative hypo- or hypertension (Mean arterial pressure < 60 mmHg or systolic blood pressure > 160 mmHg)
  • 7.Preoperative Heart rate < 45/min or > 90/min;
  • 8. Central nervous system disorder (neurologic/head trauma/uncontrolled epileptische aanvallen);

研究者

相似试验