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临床试验/NCT04544423
NCT04544423Unknown不适用

Ultrasound-guided Lumbar Erector Spinae Plane Block For Postoperative Analgesia in Knee Prosthesis

Tokat Gaziosmanpasa University1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2020年9月2日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
34
试验地点
1
主要终点
Visual analog scale

研究概览

简要总结

To determine the postoperative analgesic efficiency of ultrasound-guided lumbar erector spinae plane block, patients are divided into two groups. Study group received ultrasound-guided lumbar erector spinae plane block, where control had none. Visual analog scale and opioid consumption are recorded.

详细描述

Erector spinae plane block has successfully been demonstrated to provide an efficient analgesia in patients with rib fracture, open thoracotomy, breast surgery. The present study is aimed to investigate the intraoperative hemodynamic responses, anesthetic and analgesic consumption, and postoperative recovery quality of erector spinae plane block in patients with knee prosthesis. After approval, patients enrolled in the study are divided into two groups by computer-based randomization technique as control and study group. After standard monitorization, anesthesia induction and tracheal intubation, erector spinae plane block is performed to study group and no intervention to control group.

In the intraoperative period, 10 mg / kg paracetamol and 0.05 mg / kg morphine will be used for postoperative analgesia. After surgery, all patients will be given 10 mg/kg paracetamol every 8 hours and will be fitted with a patient-controlled analgesia (PCA) device (Tramadol HCL). PCA device bolus dose will be set to 20 mg, lock time will be set to 10 minutes and the number of buttons per hour will be set as 3.for postoperative analgesia.After surgery, VAS scores of the patients will be evaluated (in the recovery room, 1,3,6,12 and 24 hours, Patients with VAS≥4 will be given 0.03mg / kg morphine as salvage analgesia.After 30 minutes, the patients' VAS will be re-evaluated,If VAS≥4 the same dose will be repeated.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Over 18 years of age Planned to knee prosthesis An American Society of Anesthesiologists score of 1,2 or 3

排除标准

  • Severe cardiovascular disease Psychiatric diseases Rejected to participation Those who have chronic pain

结局指标

主要结局

Visual analog scale

时间窗: one time in postoperative period for one year

Visual analog scale

次要结局

  • Opioid consumption(During postoperative period for one year)

研究者

发起方
Tokat Gaziosmanpasa University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Hakan Tapar

Tokat Gaziosmanpasa University

Tokat Gaziosmanpasa University

研究点 (1)

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