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临床试验/NCT01917045
NCT01917045已完成不适用

Different Lipid Soluble Opioids for Gynecologic Laparoscopic Surgery Postoperative Patient-controlled Analgesia --- a Double Blind Randomized Study

Peking University First Hospital0 个研究点目标入组 180 人开始时间: 2012年1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
180
主要终点
visual analogue pain scores

研究概览

简要总结

The investigators noticed that Body Fat Ratio might have great influence on the efficacy of different lipid soluble anesthetics. The objective of this clinical trial was to compare the effect of that Body Fat Ratio on the efficacy of different lipid soluble anesthetics.

详细描述

The objective of this clinical trial was to compare the effect of that Body Fat Ratio on the efficacy of different lipid soluble anesthetics.

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, Care Provider)

入排标准

年龄范围
20 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • American Society of Anesthesiologists grade I-II
  • adults aged over 20 and below 50 years old,
  • non-smoker,
  • with normal hepatic and renal function.

排除标准

  • any kind of mental disorder or
  • history use of analgesics for more than 10 consecutive days,
  • asthma; and
  • those with digestion tract disorder who would get nausea or vomiting much more easily than normal people.

研究组 & 干预措施

low body fat percentage

Experimental

body fat percentage less than 30%

干预措施: Morphine (Drug)

low body fat percentage

Experimental

body fat percentage less than 30%

干预措施: Sufentanil (R30730, brand name Sufenta) (Drug)

low body fat percentage

Experimental

body fat percentage less than 30%

干预措施: Sufentanil (R30730, brand name Sufenta) + Morphine (Drug)

heigh body fat percentage

Experimental

body fat percentage more than 30%

干预措施: Sufentanil (R30730, brand name Sufenta) (Drug)

heigh body fat percentage

Experimental

body fat percentage more than 30%

干预措施: Sufentanil (R30730, brand name Sufenta) + Morphine (Drug)

heigh body fat percentage

Experimental

body fat percentage more than 30%

干预措施: Morphine (Drug)

结局指标

主要结局

visual analogue pain scores

时间窗: 24hour

we evaluate visual analogue pain scores at different time points within 24 hours after surgery

次要结局

  • nausea & vomiting(24hour)

研究者

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

ZhouYan

M.D

Peking University First Hospital

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