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临床试验/NCT02797860
NCT02797860已完成不适用

Comparison of Onset and Duration of Rocuronium Induced Neuromuscular Block Between 2nd Trimester Pregnant and Non-pregnant Women

Hallym University Kangnam Sacred Heart Hospital1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2016年6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
发起方
入组人数
90
试验地点
1
主要终点
onset time of rocuronium

研究概览

简要总结

Pregnancy is associated with major changes of the body's physiological status and composition.

These changes may modify the pharmacologic and/or pharmacokinetic profile of some drugs. Pharmacodynamic and pharmacokinetic changes in the 1st trimester during pregnancy are attributed to the following factors; Increase in plasma volume, heart rate and cardiac output; decrease in blood pressure due to decrease of systemic resistance and relative decrease of hepatic circulation and the aggravation of hepatic dysfunction. These changes intensify as pregnancy progresses into the 3rd trimester and take their effect on the onset time and duration of muscle relaxants.

Rocuronium and the steroidal non-depolarizing muscle relaxant like vecuronium is mostly excreted with bile by hepatic metabolism and classified as the FDA pregnancy category B, and is widely used in general anesthesia of pregnant women. Previous studies reported onset time of rocuronium is affected by cardiac output, blood circulation time of the whole body, and muscle perfusion. Accordingly, many researches were conducted under the assumption of onset time and duration being affected by physiologic changes during pregnancy. For example, in the research where vecuronium was used as muscle relaxant for pregnant woman undergoing C-sec, onset of vecuronium was significantly shorter than that of the control group and duration was longer. In a study investigating rocuronium used for patients right after delivery, onset time was shorter and duration was longer than that of the control group.

However, previous research mostly focused on the 3rd trimester, while there have been only a few studies of onset time and duration of rocuronium in non-obstetric surgery such as the transabdominal cervicoisthmic cerclage (TCIC) or Mcdonald surgery which are performed under general anesthesia during 2nd trimester. In this research, onset time and duration of rocuronium, which is widely used for general anesthesia in 2nd trimester pregnant females, will be compared with those of patients in the control group.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
20 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients scheduled for Transabdominal cervicoisthmic cerclage under general anesthesia or patients scheduled for elective open abdominal surgery.
  • The American Society of Anesthesiologists physical status class one or two
  • female between 20 and 45

排除标准

  • Patients with liver disease
  • Patients with kidney disease
  • Patients with Diabetes mellitus or heart disease
  • Patients with asthma or Bronchial hypersensitivity
  • Patients with a drug allergy
  • Patients BMI under 18.5 or over 27

研究组 & 干预措施

transabdominal cervicoisthmic cerclage

Second Stage of Labor pregnant women who are scheduled for transabdominal cervicoisthmic cerclage due to incompetent internal os of cervix

干预措施: Rocuronium (Drug)

control

women of childbearing age between 20 and 45

干预措施: Rocuronium (Drug)

结局指标

主要结局

onset time of rocuronium

时间窗: until T1 of Train of Four watch is suppressed to 0%,assessed up to 5 minutes

次要结局

  • duration of rocuronium(until T1 of Train of Four watch is recovered to 25%,assessed up to 1 hour)

研究者

发起方
Hallym University Kangnam Sacred Heart Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Choi Eun MI

Hallym University Kangnam Sacred Heart Hospital

Hallym University Kangnam Sacred Heart Hospital

研究点 (1)

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