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临床试验/NCT03870503
NCT03870503已完成不适用

Carbetocin Versus Oxytocin Plus Sublingual Misoprostol in the Management of Atonic Post-partum Hemorrhage (PPH) After Vaginal Delivery: a Randomized Controlled Trial

Aswan University Hospital1 个研究点 分布在 1 个国家目标入组 135 人开始时间: 2019年4月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
135
试验地点
1
主要终点
The amount of blood loss

研究概览

简要总结

The objective of this study is to compare the effectiveness and safety of carbetocin vs. oxytocin plus sublingual misoprostol in the management of atonic postpartum hemorrhage (PPH)after vaginal delivery.

详细描述

The first cause of hemorrhage at the time of delivery is uterine atony; therefore, there is general agreement that active management of the third stage of labor is recommended.

Oxytocin is the most widely used uterotonic agent but has a half-life of only 4-10 min, that is why it is better administered as a continuous intravenous infusion to achieve sustained uterotonic activity. Carbetocin is a synthetic long-acting oxytocin agonistic analog with prolonged half-life prolonging its pharmacological effects. Its prolonged uterine activity may theoretically offer advantages over oxytocin in the management of the third stage of labor. The side-effect profile of carbetocin was not found to be different from that of Oxytocin but may prove to be advantageous when compared to Syntometrine.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

This study will be a prospective double-blind randomized study

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • All participants had PPH defined as vaginal bleeding>500 ml after vaginal delivery and uterine atony confirmed by abdominal palpation

排除标准

  • gestational age<37 weeks,
  • genital tract trauma,
  • coagulation defect,
  • women with hypertension, preeclampsia, cardiac, renal or liver diseases, epilepsy
  • known hypersensitivity to carbetocin or oxytocin.

研究组 & 干预措施

oxytocin

Active Comparator

The patient will be received oxytocin 20 IU by intravenous infusion

干预措施: oxytocin (Drug)

oxytocin plus misoprostol

Active Comparator

The patient will be received oxytocin 20 IU by intravenous infusion plus 400 mc sublingual misoprostol

干预措施: oxytocin (Drug)

oxytocin plus misoprostol

Active Comparator

The patient will be received oxytocin 20 IU by intravenous infusion plus 400 mc sublingual misoprostol

干预措施: oxytocin plus misoprostol (Drug)

Carbetocin

Active Comparator

The patient will be received Carbetocin 100 mic gm IV

干预措施: Carbetocin (Drug)

结局指标

主要结局

The amount of blood loss

时间窗: 6 hours post delivery

calculation of the amount of blood loss by weighing the swabs and using pictorial charts

次要结局

  • The number of patients develop blood loss more than 1000 ml(24 hours post delivery)
  • The number of patient need blood transfusion(24 hours post delivery)

研究者

发起方
Aswan University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

hany farouk

Principal Investigator

Aswan University Hospital

研究点 (1)

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