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临床试验/NCT02219542
NCT02219542已完成4 期

Cytokines of Patients After Laparoscopic Colonic Surgery

China Medical University, China1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2014年8月最近更新:
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
80
试验地点
1
主要终点
The change of cytokine level in plasma samples

研究概览

简要总结

The investigators designed a study to determine whether with combined general-transversus abdominis plane block anesthesia or standard general anaesthetic would provide same level of cytokines in patients undergoing Laparoscopic Colonic Surgery.

详细描述

The investigators designed a study to determine whether combined general-transversus abdominis plane block anesthesia or standard general anaesthetic would provide same level of cytokine in patients undergoing Laparoscopic Colonic Surgery.

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, 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

  • •Participants were deemed eligible if they were candidates for spinal anesthesia undergoing Laparoscopic Colonic Surgery

排除标准

  • •Existing cognitive impairment as evidenced by Mini-Mental State Examination scores below 24 (of the 30 possible points)
  • A history of neurological and psychiatric diseases including stroke, and psychosis
  • Severe visual or hearing impairment
  • Unwillingness to comply with the protocol or procedures

研究组 & 干预措施

a standard general anesthesia

Placebo Comparator

a standard general anesthesia and with transversus abdominis plane block 20 ml 0.9% sodium chloride

干预措施: transversus abdominis plane block (Drug)

transversus abdominis plane block

Experimental

a standard general anesthesia with transversus abdominis plane block 20 mL 0.25% ropivacaine

干预措施: transversus abdominis plane block (Drug)

结局指标

主要结局

The change of cytokine level in plasma samples

时间窗: just after anesthesia induction ; at the end of the surgery; 24h after surgery

The blood samples were collected before induction of anesthesia and at the end of surgery.

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

Wen-fei Tan

Associate proffessor

China Medical University, China

研究点 (1)

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