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临床试验/IRCT20181107041590N1
IRCT20181107041590N1招募中3 期

Comparison the effect of interathecal injection of Dexmedetomidine plus Bupivacanie and Bupivacanie on maternal hemodynamic parameters and pain; and neonatal APGAR and arterial blood gases of women undergoing cesarean delivery under spinal anesthesia

Gorgan University of Medical Sciences0 个研究点目标入组 82 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
82

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 40 years(—)
性别
Female

入选标准

  • Pregnant women with repeated cesarean delivery and more than 39 gestational age
  • Age between 18 to 40 years old
  • Candidate for elective cesarean delivery underwent spinal anesthesia
  • American Society of Anesthesiologists (ASA) physical status classification system I and II
  • Without history of asthma, cardiovascular diseases, diabetes, acute and chronic renal failure, deep vein thrombosis, pulmonary embolism, peripheral vascular diseases, preeclampsia, eclampsia, seizure, convulsion, and cancers
  • Without history of drug abuse or sedative & hypnotic drugs
  • Without congenital malformation
  • Without history of airway problems and systemic diseases, and preterm labor
  • Without history of medication allergy
  • Without coagulopathy
  • Hemoglobin level above 10 g/dl
  • Normal level of clotting time (CT), bleeding time (BT), prothrombin time (PT), partial thromboplastin time (PTT), and international normalized ratio (INR)
  • Having at least two clinical visit with obstetrician and one blood test and 2 control sonography during pregnancy in pregnancy record
  • Filling the informed consent form

排除标准

  • Use of sedative and hypnotic drugs before surgery
  • Use of anticoagulants 48 hours before surgery
  • With psychiatric disorders

研究者

发起方
Gorgan University of Medical Sciences

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