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临床试验/IRCT20200413047056N2
IRCT20200413047056N2招募中1 期

Comparison of the effect of intrathecal injection of pethidine, pethidine-bupivacaine and bupivacaine on pain severity and hemodynamic parameters after elective cesarean section

Birjand University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
入组人数
90

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
20 years 至 40 years(—)
性别
Female

入选标准

  • ASA 1 and ASA 2 (patients with healthy or controlled mild disease) in the range of 20 to 40 years
  • No drug and smoking addiction
  • No history of hypertension, diabetes and uncontrolled comorbidities
  • Elective cesarean section
  • No chronic pain
  • No mental disorder and hysteria

排除标准

  • Emergency cesarean section
  • Placental abruption
  • Placental accreta
  • Severe bleeding during surgery
  • Drug and smoking addiction
  • Uncontrolled comorbidities
  • Take painkillers or antiemetics 24 hours before operation
  • Skin infection at the site of lumbar injection
  • History of bupivacaine or pethidine allergy
  • Change ofanesthesia type during the operation
  • Blood transfusion during the operation

研究者

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