Analgesic Efficacy of Erector Spinae Block , Quadratus Lumborum Block, and Intrathecal Morphine for Postoperative Pain Relief After Cesarean Section: A Randomized Study
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- Duration of analgesia until first analgesic request.
研究概览
简要总结
comparing analgesic efficacy of different nerve blocks on post operative cesarean sections.
详细描述
Analgesic efficacy of Erector Spinae, Quadratus Lumborum and Intrathecal Morphine for post operative pain relief after 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
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 40 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •18-40 years old
- •more or equal 37 weeks of gestation
- •Elective cesarean delivery
排除标准
- •Patient refusal
- •inability to cooperate with or understand the study
- •local infection.
- •bleeding disorder
- •known anaphylaxis to any drug used in the trial
- •ASA physical status more than 2
- •emergency operations
- •chronic opioid use (opioid use in the past 3 months)
- •Neurologic deficit or disorder
- •contraindication to regional anesthesia.
研究组 & 干预措施
Intrathcal Morphine Group
Intrathecal morphine administration for post operative pain relief after cesarean section
干预措施: Intrathcal Morphine Group (Procedure)
Quadratus Lumborum nerve block group
Quadratus Lumborum nerve block administration for post operative pain relief after cesarean section
干预措施: Quadratus Lumborum nerve block(QL) group (Procedure)
Erector Spinae nerve block group
Erector Spinae nerve block administraion for post operative pain relief after cesarean section
干预措施: Erector Spinae nerve block (ESP)group (Procedure)
结局指标
主要结局
Duration of analgesia until first analgesic request.
时间窗: 24 hours .
the time interval from immediate postoperative period until NRS reached 4
次要结局
未报告次要终点
研究者
Mahmoud Mamdouh Ekram
principal investigator.
Assiut University