跳至主要内容
临床试验/TCTR20201204002
TCTR20201204002已完成3 期

Study of surgical site infection with or without prophylactic oral antibiotics

rmia University of Medical Sciences0 个研究点目标入组 462 人开始时间: 2020年12月4日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
462

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
0 N/A (No limit) 至 0 N/A (No limit)(—)
性别
All

入选标准

  • All participants with emergency cesarean section, satisfied to participate without any sensitivity to antibiotics.

排除标准

  • Exclusion criteria were receiving antibiotics in addition to routine cefazolin, intraoperative atony event, placenta previa, decolonization, massive bleeding leading to blood transfusion, BMI> 35 kg/m2, taking immunosuppressive drugs and corticosteroids, known underlying diseases including autoimmune, lymphoblastic, rheumatological and cardiac diseases, elective cesarean section, febrile patients at the time of hospitalization

研究者

发起方
rmia University of Medical Sciences

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