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临床试验/NCT04547608
NCT04547608已完成不适用

The Impact of the Timing of Rocuronium After Induction With Propofol on Temporal Summation of Pain in Gynecologic Laparoscopic Surgery-prospective and Controlled Study.

Wonkwang University Hospital2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
2
主要终点
the grade of rocuronium induced withdrawal movement.

研究概览

简要总结

Temporal summation of pain, which is defined as the perception of increasingly greater pain evoked by repetitive painful stimuli, is highly variable between individuals. This study aimed to determine the impact of the timing of rocuronium after induction with propofol on temporal summation of pain in gynecologic laparoscopic surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

盲法说明

Attending anesthesiologist knew which anesthetic agents were used. However Outcomes assessor didn't know which anesthetic agents were used.

入排标准

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

入选标准

  • Elective gynecologic laparoscopic surgery
  • American Society of Anesthesiologists' physical status class) I-II

排除标准

  • Menopause (to exclude the hormonal effect on pain)
  • Patients who had muscular, cardiovascular, hepatic or kidney disorders and patients with a history of medication who would affect muscle relaxants were excluded from this study.
  • Patients with difficult venous access on forearm, a known allergy to propofol or rocuronium, chronic pain, pregnancy, and those who had received analgesics or sedatives within the previous 24 hours, were excluded from the study.

结局指标

主要结局

the grade of rocuronium induced withdrawal movement.

时间窗: during anesthesia induction

withdrawal movements were graded by the investigator according to the following scale: 1. - no pain (no response); 2. - mild pain (movement at wrist only); 3. - moderate pain (movement involving the arm only with elbow or shoulder); 4. - severe pain (generalized response or movement in more than one extremity

次要结局

  • visual analog scale (VAS) for injection pain(during anesthesia induction)
  • VAS for pain(at 1 hour, 24 hours and 48 hours)
  • Patient controlled analgesia (PCA) Opioid consumption(at 24 and 48 hours)

研究者

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

Cheol Lee

Professor

Wonkwang University Hospital

研究点 (2)

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