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Carbetocin at Elective Cesarean Deliveries: A Dose-finding Study in Women With BMI ≥ 40kg/m2

Postpartum hemorrhage (PPH) due to uterine atony is a major cause of maternal morbidity and mortality. Carbetocin is a uterotonic with a superior pharmacokinetic profile to oxytocin. In a study performed at Mount Sinai Hospital, the investigators have shown that smaller doses of carbetocin (14.8 mcg) are as effective in achieving adequate uterine tone at elective cesarean section compared to the current recommended dose of 100mcg. However, this study was limited to those women with a body mass index (BMI) of <40 kg/m2. Maternal obesity has been shown to increase the risks of hemorrhage secondary to uterine atony, therefore the investigators wish to perform a dose finding study to determine the ED90 of carbetocin at caesarean section in those women with a BMI>40.

研究概览

地位

完全的

条件

干预/治疗

详细说明

Postpartum hemorrhage (PPH) is one of the leading causes of death during childbirth and accounts for an estimated 140,000 deaths per year worldwide. The World Health Organization (WHO) recommends active management of the third stage of labor to prevent PPH, even in low risk patients. Prophylactic uterotonic drugs administered after delivery are the main element of active management of the third stage and have been demonstrated to reduce the incidence of PPH by up to 40%.

Oxytocin is the most commonly used uterotonic in North America, however it has a very short duration of action and requires a continuous infusion to achieve sustained effect, with large doses associated with adverse effects like low blood pressure, nausea, vomiting, abnormal heart rhythms and changes on ECG. Carbetocin is a synthetic oxytocin analogue. It causes uterine contraction via the same mechanism as oxytocin. Its duration of action is 4 to 7 times that of oxytocin due to an increased biological half-life in plasma and at the oxytocin receptors in the uterus. The Society of Obstetricians and Gynecologists of Canada (SOGC) has recommended a single dose of 100 mcg of carbetocin at elective cesarean delivery to promote uterine contraction. In a study performed at Mount Sinai Hospital, the investigators have shown that smaller doses of carbetocin (14.8 mcg) are effective in achieving adequate uterine tone at elective cesarean section. However this study was limited to those women with a BMI of <40 kg/m2

The prevalence of obesity is increasing in young women and some studies have shown that obese women have higher rates of caesarean delivery compared to non-obese women. Other studies have demonstrated an increased risk of hemorrhage due to poor uterine tone in obese women. Laboratory studies show that BMI alone appears to contribute to blunted uterine muscle responses and therefore contraction responses to oxytocin in obese women. Previous dose finding studies have excluded those women with a BMI of ≥40kgm2. Therefore, the investigators wish to perform a double-blind dose finding study using the biased coin up-and-down sequential allocation technique to determine the ED90 of carbetocin at caesarean section in those women with a BMI>40.

研究类型

介入性

注册 (实际的)

30

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Ontario
      • Toronto、Ontario、加拿大、M5G1X5
        • Mount Sinai Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 50年 (成人)

接受健康志愿者

是的

有资格学习的性别

女性

描述

Inclusion Criteria:

  • BMI ≥40kg/m2
  • Elective cesarean delivery under regional anesthesia
  • Gestational age ≥ 37 weeks
  • No known additional risk factors for postpartum hemorrhage
  • Written informed consent to participate in this study

Exclusion Criteria:

  • Refusal to give written informed consent
  • Allergy or hypersensitivity to carbetocin or oxytocin
  • Conditions (other than high BMI) that may predispose to uterine atony and postpartum hemorrhage such as placenta previa, multiple gestation, polyhydramnios, uterine fibroids, previous history of uterine atony and postpartum bleeding, or bleeding diathesis.
  • Hepatic, renal, and vascular disease
  • Use of general anesthesia prior to the administration of the study drug

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
有源比较器:Carbetocin 10mcg
Patient is given 10 mcg of carbetocin intravenously over 1 minute, immediately upon delivery of the fetal head.
carbetocin administered IV, over 1 minute following delivery of the fetal head
其他名称:
  • 耐力霉素
有源比较器:Carbetocin 20mcg
Patient is given 20 mcg of carbetocin intravenously over 1 minute, immediately upon delivery of the fetal head.
carbetocin administered IV, over 1 minute following delivery of the fetal head
其他名称:
  • 耐力霉素
有源比较器:Carbetocin 40mcg
Patient is given 40 mcg of carbetocin intravenously over 1 minute, immediately upon delivery of the fetal head.
carbetocin administered IV, over 1 minute following delivery of the fetal head
其他名称:
  • 耐力霉素
有源比较器:Carbetocin 60mcg
Patient is given 60 mcg of carbetocin intravenously over 1 minute, immediately upon delivery of the fetal head.
carbetocin administered IV, over 1 minute following delivery of the fetal head
其他名称:
  • 耐力霉素
有源比较器:Carbetocin 80mcg
Patient is given 80 mcg of carbetocin intravenously over 1 minute, immediately upon delivery of the fetal head.
carbetocin administered IV, over 1 minute following delivery of the fetal head
其他名称:
  • 耐力霉素
有源比较器:Carbetocin 100mcg
Patient is given 100 mcg of carbetocin intravenously over 1 minute, immediately upon delivery of the fetal head.
carbetocin administered IV, over 1 minute following delivery of the fetal head
其他名称:
  • 耐力霉素

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
术中需要额外的子宫收缩药物
大体时间:1小时
由于出血或子宫张力差,进行剖宫产的产科医生要求额外使用宫缩药物。
1小时

次要结果测量

结果测量
措施说明
大体时间
低血压:收缩压低于基线的 80%
大体时间:2小时
收缩压 < 基线的 80%,从给药到手术结束
2小时
心动过速:心率大于基线的 130%
大体时间:2小时
心率 > 基线的 130%,从给药到手术结束
2小时
心动过缓:心率低于基线的 70%
大体时间:2小时
从给药到手术结束,心率 < 基线的 70% 或心率 < 50bpm
2小时
室性心动过速的存在:心电图
大体时间:2小时
心电图记录的室性心动过速的存在,从给药到手术结束
2小时
房颤的存在:心电图
大体时间:2小时
心电图记录的心房颤动的存在,从给药到手术结束
2小时
心房扑动的存在:心电图
大体时间:2小时
心电图记录的心房扑动的存在,从给药到手术结束
2小时
恶心的存在:调查问卷
大体时间:2小时
恶心的存在和发作次数,从给药到手术结束,由患者报告
2小时
呕吐的存在:调查问卷
大体时间:2小时
呕吐的存在和发作次数,从给药到手术结束
2小时
胸痛的存在:调查问卷
大体时间:2小时
患者报告的从给药到手术结束期间出现的任何胸痛
2小时
呼吸急促的存在:调查问卷
大体时间:2小时
患者报告的从给药到手术结束期间出现的任何呼吸急促
2小时
头痛的存在:调查问卷
大体时间:2小时
患者报告的从给药到手术结束期间出现的任何头痛
2小时
潮红的存在:调查问卷
大体时间:2小时
任何潮红的存在,从给药到手术结束
2小时
估计失血量
大体时间:24小时
失血量将通过手术前和剖宫产后 24 小时评估的血细胞比容值的差异来计算。
24小时
手术期间静脉输液
大体时间:2小时
从进入手术室到皮肤闭合的输液总量(ml)。
2小时
Uterine tone 2 minutes
大体时间:2 minutes
Uterine tone, defined as satisfactory or unsatisfactory by the obstetrician at 2 minutes after completion of the carbetocin injection.
2 minutes
Uterine tone 5 minutes
大体时间:5 minutes
Uterine tone, defined as satisfactory or unsatisfactory by the obstetrician at 5 minutes after completion of the carbetocin injection.
5 minutes
Additional uterotonics administered
大体时间:45 minutes
The drug, dosage and timing of any additional uterotonic medication given during surgery.
45 minutes

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2018年11月19日

初级完成 (实际的)

2019年5月16日

研究完成 (实际的)

2019年5月17日

研究注册日期

首次提交

2018年9月13日

首先提交符合 QC 标准的

2018年9月13日

首次发布 (实际的)

2018年9月14日

研究记录更新

最后更新发布 (实际的)

2019年6月7日

上次提交的符合 QC 标准的更新

2019年6月6日

最后验证

2019年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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