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临床试验/NCT02146638
NCT02146638已完成不适用

Post Operative Pain Control: Continuous Infusion of Morphine vs Fentanyl. Clinical Outcomes

Catholic University of the Sacred Heart1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2012年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
pain scores

研究概览

简要总结

Aim of this study is to compare benefits and disadvantages in using continuous infusion of morphine or fentanyl for post operative analgesia.

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
Double (Participant, Investigator)

入排标准

年龄范围
35 Years 至 59 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • ASA 1 or 2 patients
  • undergoing major gynaecological surgery

排除标准

  • age > 60 years
  • obesity (BMI>30 Kg/m2)
  • cardiac and respiratory diseases
  • renal impairment
  • liver disorders
  • allergies to any drug used in the study

研究组 & 干预措施

Morphine

Active Comparator

Patients received morphine 0.02 mg/Kg/h infused at 2 ml/h for 24 hours. The infusion contained morphine and saline.

干预措施: Morphine (Drug)

Fentanyl

Experimental

Patients received Fentanyl 0.3 mcg/Kg/h infused at 2 ml/h for 24 hours. The infusion contained morphine and saline.

干预措施: Fentanyl (Drug)

结局指标

主要结局

pain scores

时间窗: data were recorded during the 24 post operative hours

data were recorded at 1,6,18 and 24 hours after surgery

次要结局

  • analgesic requirements(during the 24 hours after surgery)

研究者

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

Francesca Bevilacqua

medical doctor

Catholic University of the Sacred Heart

研究点 (1)

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