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临床试验/IRCT2013080710511N2
IRCT2013080710511N2已完成2 期

Comparison of prophylactic administration of cefazolin, ampicillin and azithromycin in prevention of postpartum infections after cesarean

Arak University of Medical Sciences0 个研究点目标入组 375 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
375

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

  • Inclusion criteria were:
  • Non-elective Caesarean section women candidates; Gestational age of 28 weeks and more.
  • Exclusion criteria were:
  • Sensitivity to cefazolin or ampicillin or azithromycin; Unwillingness of patients; Received systemic antibiotics within 2 last weeks; Fever prior cesarean; PROM more than 18 hours; chorioamnionitis; Receiving immunosuppressive drugs; Diseases such as diabetes and immune deficiency: liver disease, kidney disease and heart failure or pulmonary edema; multiple pregnancies; preeclampsia; Urinary tract infection or pneumonia; Operation for more than an hour; Intraoperative subcutaneous drains; Abnormal adherence of the placenta to be observed during operation; Elective caesarean; Diarrhea at the time of delivery; Any patient with significant electrolyte disturbances such as hypokalemia, hypocalcemia.

排除标准

  • 未提供

研究者

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