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临床试验/NCT03060070
NCT03060070已完成2 期

Comparison of the Analgesic Effect of Ketamine Versus Dexmedetomidine Added to Local Anesthetic in TAP Block for Lower Abdominal Cancer Surgery

Assiut University1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2017年3月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
90
试验地点
1
主要终点
postoperative rescue morphine consumption

研究概览

简要总结

Comparing the analgesic effects of ketamine and dexmedetomidine when added to local anesthetic in TAP block for postoperative analgesia after lower abdominal cancer surgery.

研究设计

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

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients ASA I and II to whom abdominal surgery for cancer will be conducted will be included in the study

排除标准

  • Coagulopathies
  • ASA III or IV, patient refusal, sensitivity to the used drugs

研究组 & 干预措施

control group,

Placebo Comparator

saline in the same volume will be added to the local anesthetic for TAP block in patients undergoing abdominal cancer surgery

干预措施: Ketamine (Drug)

control group,

Placebo Comparator

saline in the same volume will be added to the local anesthetic for TAP block in patients undergoing abdominal cancer surgery

干预措施: dexmedetomidine (Drug)

ketamine group,

Active Comparator

ketamine in a dose of 0.5mg/kg will be added to the local anesthetic for TAP block in patients undergoing abdominal cancer surgery

干预措施: dexmedetomidine (Drug)

ketamine group,

Active Comparator

ketamine in a dose of 0.5mg/kg will be added to the local anesthetic for TAP block in patients undergoing abdominal cancer surgery

干预措施: control group (Drug)

dexmedetomidine group

Active Comparator

dexmedetomidine in a dose of 1ug/kg will be added to the local anesthetic for TAP block in patients undergoing abdominal cancer surgery

干预措施: Ketamine (Drug)

dexmedetomidine group

Active Comparator

dexmedetomidine in a dose of 1ug/kg will be added to the local anesthetic for TAP block in patients undergoing abdominal cancer surgery

干预措施: control group (Drug)

结局指标

主要结局

postoperative rescue morphine consumption

时间窗: 24 hours postoperative

postoperative rescue morphine consumption

次要结局

未报告次要终点

研究者

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

Ahmed H Othman

Associte professor

Assiut University

研究点 (1)

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