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临床试验/IRCT20211012052747N1
IRCT20211012052747N1招募中3 期

Comparative Study of Fentanyl vs Dexmedetomidine as Adjuvants to Intrathecal Bupivacaine on post oprative pain in Cesarean Section

Birjand University of Medical Sciences0 个研究点目标入组 120 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
120

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 35 years(—)
性别
Female

入选标准

  • Having informed consent to enter the study
  • ASA Class 1 and 2
  • Term pregnancy
  • Non-emergency cesarean section

排除标准

  • Drug addiction
  • Dissatisfaction with spinal anesthesia
  • Duration of surgery more than 1 hour
  • Pregnancy with ASA 3 and above
  • Patients with head trauma
  • Patients with spinal deformity
  • Inability to position the patient
  • Infection in site of spinal anesthesia
  • Hypersensitivity to local anesthetic drugs
  • Coagulation disorders and heart valve problems (especially AS)

研究者

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