跳至主要内容
临床试验/IRCT20230316057741N1
IRCT20230316057741N1尚未招募3 期

Evaluation of the effect of ketamine with gabapentin on the severity of some complications of spinal anesthesia in cesarean section

Yasouj 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
尚未招募
发起方
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 34 years(—)
性别
Female

入选标准

  • No emergency C/S surgery
  • No emergency C/S surgery
  • No emergency C/S surgery
  • Type of surgical incision on the skin of Von Stilweber on the uterus, transverse incision on the lower uterine segment (kerr)
  • Absence of underlying disease such as weak immune system, diabetes, high blood pressure, cardiopulmonary disease, blood disease, autoimmune disease, severe liver hepatitis, asthma, pancreatitis, or coagulation disorders.
  • Singleton pregnancy
  • Not taking special medicine
  • Gestational age greater than or equal to 28 weeks
  • Being in the low risk group based on the risk factors of PPH, including placenta previa, placental abruption, hypertension, HELLP syndrome, macrosomia, non-cephalic presentation, intrauterine infection or the use of assisted reproductive technology (ART).
  • Mother's BMI based on pre-pregnancy weight less than 30 kg/m2
  • Natural plt counting

排除标准

  • Any contraindications for spinal anesthesia
  • Any contraindications to receiving ketamine or gabapentin
  • Severe bleeding during C/S
  • If any of the patients in the placebo group suffer from any of the side effects that cannot be tolerated by the patient, the patient will be treated for the side effects with the opinion of the relevant specialist, and the patient will be excluded from the study.

研究者

发起方
Yasouj University of Medical Sciences

相似试验