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临床试验/PACTR201910644489698
PACTR201910644489698已完成未知

Tranexamic acid versus Misoprostol in reducing blood loss during cesarean section: a cross-sectional comparative study in Abakaliki, Nigeria

Christian O OGAH0 个研究点目标入组 358 人开始时间: 2019年10月8日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
358

研究概览

简要总结

The maternal demographic and obstetrics factors and blood loss determinants like bedside clotting time, duration of surgery and cadre of surgeon during cesarean section were statistically non-significant between the two groups. Mean intraoperative blood loss was not significantly different between the misoprostol group and tranexamic acid group (547 ± 183.75ml vs. 551.66 ± 21.74ml, P = 0.519). The mean difference in PCV changes was not significant between the groups (2.41±0.95% vs. 2.29±0.56%, P = 0.463). Side effect profile was similar for both groups except shivering which was statistically higher among the misoprostol group compared to the tranexamic acid group (RR = 0.70; 95%CI 0.40 - 0.91, P = 0.028). From this study, tranexamic acid was comparable to misoprostol in the reduction of blood loss during cesarean section. Therefore, tranexamic acid could act as a good alternative to misoprostol for prophylaxis for blood loss during elective cesarean section.

研究设计

研究类型
Interventional

入排标准

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
Female

入选标准

  • Booked women
  • Elective cesearean section

排除标准

  • Previous cesarean section
  • Hypertensive disorders of pregnancy
  • Known allergy to misoprostol or tranexamic acid
  • Antepartum haemorrhage
  • Emergency caesarean section
  • Bleeding disorder

研究者

发起方
Christian O OGAH

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