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临床试验/IRCT20141009019470N80
IRCT20141009019470N80已完成2 期

The comparison of intravenous dexamethasone and paracetamol in the prevention of post Dural puncture headache in elective cesarean section under spinal anesthesia

Shiraz University of Medical Sciences0 个研究点目标入组 290 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
入组人数
290

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
no limit 至 no limit(—)
性别
Female

入选标准

  • Minimum NPO time = 8 hours
  • Elective cesarean section

排除标准

  • Spinal anesthesia
  • Contraindications of Local infection in the lumbar region (spinal cord needle entry site)
  • Use anti-platelet and anticoagulant
  • Sensitivity to Local anesthesia
  • Diabetes mellitus
  • kidney Diseases
  • Renal failure
  • Coagulation disorder
  • Liver disease
  • Heart disease
  • History of seizure or any neurological disease
  • Migraine and pressure headaches
  • The history of drug addiction
  • Failure of spinal anesthesia or multiple attempts to perform spinal anesthesia more than once
  • Systolic blood pressure above 150 and less than 100
  • Preeclampsia
  • The lack of proper growth of the uterus
  • Weight above 100
  • Height less than 150 and more than 180 cm
  • Hemoglobin less than 8
  • Caesarean section more than 3 times
  • Sensitivity to dexamethasone and paracetamol

研究者

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