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临床试验/NL-OMON52953
NL-OMON52953招募中4 期

The impact of neuromuscular relaxation and nociception guided anaesthesia on hemodynamic variables during abdominal laparoscopic surgery: a strategy trial. - RELAX-LAP

eids Universitair Medisch Centrum0 个研究点目标入组 50 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
招募中
入组人数
50

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 64(—)

入选标准

  • Scheduled for laparoscopic or robotic abdominal surgery
  • Ability to give oral and written consent

排除标准

  • Known or suspected neuromuscular disorders impairing neuromuscular function;
  • Allergies to muscle relaxants, anesthetics or narcotics;
  • A (family) history of malignant hyperthermia;
  • Women who are or may be pregnant;
  • Preexisting cardiac disease (any);
  • Untreated or uncontrolled hypertension;
  • COPD gold 3 or higher
  • Any contradictions for TEE:
  • Preexistent esophageal pathology (stricture, tumor, diverticulum)
  • Any increased risk factor for upper gastro intestinal tract bleed:
  • History of GI surgery;
  • History of GI bleed;
  • Esophageal varices;
  • Gastric or esophageal inflammation;
  • Severe thrombocytopenia (less than 50k) or severely elevated INR (>4).

研究者

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