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临床试验/NCT05679375
NCT05679375已完成4 期

Comparison Between the Analgesic Effects of Intrathecal Versus Intravenous Ketamine After Spinal Anaesthesia for Elective Caesarean Delivery :a Randomised Trial

Assiut University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年2月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
60
试验地点
1
主要终点
Time to the first analgesic request

研究概览

简要总结

In the current study, the investigators will compare the effects of low-dose intravenous (i.v.) ketamine versus intrathecal Ketamine added to spinal anesthesia on the time to first request for analgesia and maternal pain scores and overall satisfaction in patients undergoing cesarean section.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

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

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Intrathecal Ketamine

Active Comparator

Patients will receive intrathecal Ketamine 0.1mg/kg added to bupivacaine and morphine.

干预措施: Intrathecal ketamine (Drug)

Intravenous ketamine

Active Comparator

Patients will receive IV Ketamine 0.25mg/kg after spinal anesthesia with bupivacaine and morphine.

干预措施: Intravenous ketamine (Drug)

结局指标

主要结局

Time to the first analgesic request

时间窗: First Postoperative day

次要结局

  • Postoperative pain scores NRS at rest and on movement; (2, 4, 6, 12, and 24 hours) postoperative(first postoperative day)

研究者

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

Youstina Tharwat Sedky

Principal investigator

Assiut University

研究点 (1)

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IV and Intrathecal Ketamine in Cesarean Section | 临床试验