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临床试验/NCT04822870
NCT04822870Unknown不适用

Comparison of Ultrasound-guided Quadratus Lumborum Block and Iliohypogastric/Ilioinguinal Nerve Block for Postoperative Pain Management in Patients Undergoing Cesarean Section: a Randomized Double-blind Clinical Trial Study

Peking University People's Hospital1 个研究点 分布在 1 个国家目标入组 87 人开始时间: 2021年3月31日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
87
试验地点
1
主要终点
morphine consumption

研究概览

简要总结

The purpose of this study is to compare the analgesic effect of ultrasound-guided quadratus lumborum block and iliohypogastric/ilioinguinal nerve block for postoperative pain management in patients undergoing cesarean section.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • •singleton pregnancy
  • •gestation of at least 37 weeks
  • •American Society of Anesthesiologists (ASA) physical status I or II
  • •finish Pfannenstiel section under combined spinal and epidural anesthesia

排除标准

  • •pruritus existed before the surgery
  • •allergic to lidocaine, ropivacaine or dexamethasone

研究组 & 干预措施

quadratus lumborum block

Experimental

Parturients receive ultrasound-guided quadratus lumborum block as post-operative analgesia.

干预措施: quadratus lumborum block (Procedure)

iliohypogastric/ilioinguinal nerve block

Experimental

Parturients receive ultrasound-guided iliohypogastric/ilioinguinal nerve block as post-operative analgesia.

干预措施: iliohypogastric/ilioinguinal nerve block (Procedure)

epidural analgesia

Active Comparator

Parturients receive epidural morphine via epidural catheter placed during anesthesia as post-operative analgesia.

干预措施: epidural analgesia (Procedure)

结局指标

主要结局

morphine consumption

时间窗: 24 hours postoperatively

Every parturient use a patient-controlled intravenous analgesia pump as supplement for the interventions. The analgesia pump contains morphine and can record morphine consumption. Postoperative use of morphine can reflect analgesic effect.

次要结局

  • morphine consumption(48 hours postoperatively)
  • effective analgesia time(48 hours postoperatively)
  • satisfaction score(48 hours postoperatively)
  • hospital stay(at discharge assessed up to 10 days)
  • pain score(48 hours postoperatively)
  • adverse effect(48 hours postoperatively)
  • hospitalize cost(at discharge assessed up to 10 days)
  • morphine consumption(6 hours postoperatively)
  • morphine consumption(12 hours postoperatively)
  • pain score(6 hours postoperatively)
  • pain score(12 hours postoperatively)
  • pain score(24 hours postoperatively)
  • adverse effect(6 hours postoperatively)
  • adverse effect(12 hours postoperatively)
  • adverse effect(24 hours postoperatively)

研究者

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

Yi Feng, MD

Head of Anesthesiology

Peking University People's Hospital

研究点 (1)

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