跳至主要内容
临床试验/NCT04675840
NCT04675840已完成不适用

Intrathecal Morphine for Robotic-assisted Laparoscopic Hysterectomy- a Prospective Randomized Controlled Study.

Karlstad Central Hospital2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100
试验地点
2
主要终点
Postop grade of nausea & vomiting

研究概览

简要总结

Is there any difference in the intensity of postoperative pain, nausea, urinary retention and legth of hospital stay in patients undergoing robotic assisted laparoscopic surgery if they receive intrathecal morphine or peroral and intravenous opiates during the surgery and is there a significant difference in the need of opiates after the 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
Single (Investigator)

入排标准

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

入选标准

  • * Patients accepted for robotic-assisted laparoscopic surgery

排除标准

  • Coagulopathy,
  • Prior spine surgery,
  • Chronic pain problems,
  • Drug abuse,
  • Pregnancy
  • < 18 years

结局指标

主要结局

Postop grade of nausea & vomiting

时间窗: First 24 hours after surgery

Amount of antemetics given

Postop morphine consumption

时间窗: First 48 hours after surgery

Amount of opiates given postop

次要结局

  • Hospital length of stay.(Up to 7 days)
  • Patient overall satisfaction score.(Up to 7 days.)

研究者

发起方
Karlstad Central Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ragnar Henningsson

Associate Professor

Karlstad Central Hospital

研究点 (2)

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