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临床试验/NCT06089200
NCT06089200已完成2 期

Comparison of Post-operative Analgetics With Transversus Abdominis Block and Spinal Morphine for Post-Caesarean Section: A Randomised Trial Study

Universitas Padjadjaran2 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2023年2月23日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
44
试验地点
2
主要终点
Length of time the patient needed the first additional opioid analgesics

研究概览

简要总结

The goal of this randomized controlled trial is to compare the effect of TAP block vs spinal morphine for post caesarean section analgesics. The main questions it aims to answer are:

  • Which post op analgesic method works better for patients who underwent caesarean section
  • The number of additional opioid needed

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
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Indicated for caesarean section as assessed by Obstetricians
  • Consented to be included in the study

排除标准

  • Allergy history
  • Spinal converted to general anesthesia

结局指标

主要结局

Length of time the patient needed the first additional opioid analgesics

时间窗: 24 hours post operative

Total need for additional opioids

时间窗: 24 hours post operative

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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