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临床试验/TCTR20190702006
TCTR20190702006已完成未知

Comparison between Continuously Intravenous Low dose and Intermittently Intramuscular Administration of Ketamine to Reduce Postoperative Pain in Onco-gynecologic Patients.

-0 个研究点目标入组 40 人开始时间: 2019年7月2日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 65 Years(—)
性别
Female

入选标准

  • Inclusion criteria
  • •Age between18-65 years old
  • •ASA physical status 1-3
  • •Operation time more than 1 hours
  • •Patients able to use PCA device for postoperative pain

排除标准

  • Exclusion criteria
  • •Documented of contraindication for ketamine used
  • •history of drug allergy to morphine, fentanyl, ketamine.
  • •Suspected to remain intubation for postoperative period.
  • •Severe co-morbidity cardiovascular disease.
  • •Renal insufficiency
  • •History of drug addicted or psychological problem.
  • •underlying hematotological disease due to contraindication for intramuscular injection

研究者

发起方
-

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