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临床试验/NCT02362022
NCT02362022已完成4 期

Comparison of Two Different Doses of Intravenous Morphine on Desflurane Consumption and Recovery Time in Patients Undergoing Total Abdominal Hysterectomy

Baskent University1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2007年9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
90
试验地点
1
主要终点
postoperative desflurane consumption

研究概览

简要总结

Combination of volatile and opioid agents are used to achieve unconsciousness, haemodynamic stability and analgesia for surgical prosedures. This prospective, randomized, double-blind, controlled study evaluates the effects of two different doses of morphine sulphate (0.1 mg/kg and 0.2 mg/kg), on desflurane consumption, recovery characteristics, postoperative analgesic requirements and side effects during total abdominal hysterectomy.

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 (Care Provider, Investigator)

入排标准

年龄范围
40 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • undergoing total abdominal hysterectomy with general anaesthesia

排除标准

  • renal dysfunction (cre>1.2), liver failure, cardiovascular, psychiatric, allergic and metabolic disorders

研究组 & 干预措施

Group Saline

Placebo Comparator

Group Saline (Group S) received i.v saline 0.9 % in 10 ml volume (n=30)

干预措施: Morphine (Drug)

Group Morphine 1

Active Comparator

Group Morphine 1 (Group M1) received i.v morphine 0.1 mg kg-1, in 10 ml volume (n=30)

干预措施: Morphine (Drug)

Group Morphine 2

Active Comparator

Group Morphine 2 (Group M2) received i.v morphine 0.2 mg kg-1, in 10 ml volume (n=30)

干预措施: Morphine (Drug)

结局指标

主要结局

postoperative desflurane consumption

时间窗: postoperative first hour

sedation scores for OASS scale

时间窗: postoperative first hour

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

CAGLA BALI,MD

medical doctor

Baskent University

研究点 (1)

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