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临床试验/NCT04277611
NCT04277611已完成不适用

Comparison Between Ultrasound Guided Subcostal Oblique Quadratus Lumborum Block and Erector Spinae Plane Block in Patients Undergoing Percutaneous Nephrolithotomy

Assiut University2 个研究点 分布在 1 个国家目标入组 92 人开始时间: 2021年4月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
92
试验地点
2
主要终点
Analgesia

研究概览

简要总结

comparing the subcostal oblique Quadratus Lumborum block and the Erector Spinae plane block in patients undergoing percutaneous nephrolithotomy operation to get the best and longest postoperative analgesic effect.

详细描述

Here the investigators are going to compare between the Anterior approach for the subcostal oblique Quadratus Lumborum block (QLB) and the Erector Spinae Plane Block (ESPB) to determine their level of spread and their value in controlling postoperative pain in patients scheduled for Percutaneous Nephrolithotomy surgery. We hypothesized that quadratus lumborum is not inferior regarding the duration of analgesia when compared to erector spinae in patients undergoing percutaneous nephrolithotomy under general anesthesia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age: 18-60
  • ASA (American Society of Anesthesiologists) class I and II
  • Elective surgery
  • Patients undergoing PNL surgery

排除标准

  • Patient's refusal
  • Allergy or contraindications to drugs used in the study
  • Emergency surgery
  • Psychiatric disorders
  • Severely co-morbid patients
  • Inflammation or infection over injection site
  • Bleeding diathesis; INR more than 1.5 and Platelet count less than 100,000/mm3
  • Peripheral neuropathy
  • Obese patients BMI ≥35
  • Patients on previous opioid therapy
  • Pre-operative haemoglobin <10 mg/dl
  • Inability to properly describe postoperative pain to investigators
  • Coagulation abnormalities
  • History of drug addiction or alcohol abuse
  • History of Previous renal surgery

结局指标

主要结局

Analgesia

时间窗: 48 hours

Total opioid consumption during the first 48hours postoperatively.

次要结局

  • time of recovery of bowl movement(5 days postoperative)
  • postoperative length of hospital stay(within 2 weeks postoperative.)
  • Pain Scores using Visual Analog Scale (VAS) Scores(24 hours postoperative.)
  • ambulation time(5 days postoperative)
  • Analgesia(24 hours)
  • episodes of nausea and vomiting(within 24 hours postoperative)
  • patient satisfaction with anesthesia(48 hours postoperative.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Peter Bassem Halim Gadelsyed

Resident Doctor in Anesthesia, postoperative ICU and pain management department

Assiut University

研究点 (2)

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