Carbetocin at Elective Cesarean Deliveries: A Dose-finding Study in Women With BMI ≥ 40kg/m2
研究概览
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
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
-
-
Ontario
-
Toronto、Ontario、加拿大、M5G1X5
- Mount Sinai Hospital
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
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
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:
|
|
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:
|
|
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:
|
|
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:
|
|
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:
|
|
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:
|
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
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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.