Postpartum Hemorrhage Clinical Trial
Official title:
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.
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.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03434444 -
In Vitro Optimization of Oxytocin-induced Myometrial Contractility by Propranolol
|
N/A | |
Terminated |
NCT01980173 -
Medico-economic Comparison of Postpartum Hemorrhage Management Using the Bakri Balloon and Standard Care
|
N/A | |
Not yet recruiting |
NCT06033170 -
Celox™ PPH for Reaching Haemostasis in Patients With Postpartum Hemorrhage
|
N/A | |
Not yet recruiting |
NCT02319707 -
Management of the Third Stage of Labor
|
Phase 3 | |
Completed |
NCT02163616 -
Treatment of Postpartum Hemorrhage With Misoprostol: Fever Study
|
Phase 3 | |
Recruiting |
NCT01600612 -
Oxytocin, Carbetocin and Misopristol for Treatment of Postpartum Hemorrhage: A Multicentric Randomized Trial
|
N/A | |
Completed |
NCT02079558 -
Efficacy of Oxytocin vs. Carbetocin in Prevention of Postpartum Hemorrhage After Cesarean Section
|
Phase 2 | |
Withdrawn |
NCT01108302 -
Effectiveness, Safety and Feasibility of Auxiliary Nurse Midwives' (ANM) Use of Oxytocin in Uniject™ to Prevent Postpartum Hemorrhage in India
|
N/A | |
Completed |
NCT00097123 -
RCT of Misoprostol for Postpartum Hemorrhage in India
|
N/A | |
Completed |
NCT02883673 -
Safety and Effectiveness of the Jada System in Treating Primary Postpartum Hemorrhage
|
N/A | |
Completed |
NCT02542813 -
Safety, Tolerability and Pharmacokinetics (PK) Study of Oxytocin (GR121619) Administered Via an Inhaled Route in Healthy Female Volunteers
|
Phase 1 | |
Completed |
NCT04201665 -
EMG for Uterotonic Efficiency Estimation
|
N/A | |
Terminated |
NCT03246919 -
Ideal Time of Oxytocin Infusion During Cesarean Section
|
Phase 4 | |
Not yet recruiting |
NCT05501106 -
Reducing Postpartum Hemorrhage After Vaginal Delivery
|
N/A | |
Completed |
NCT05429580 -
Prophylactic Tranexamic Acid Use After Vaginal Delivery
|
N/A | |
Terminated |
NCT03064152 -
Rotational Thromboelastometry for the Transfusion Management of Postpartum Hemorrhage After Vaginal or Cesarean Delivery
|
N/A | |
Recruiting |
NCT05382403 -
Novel Vacuum-Induced Hemorrhage Control for Postpartum Hemorrhage
|
N/A | |
Completed |
NCT03344302 -
Oxytocin Administration During Cesarean Section
|
Phase 4 | |
Completed |
NCT02805426 -
Effectiveness of Tranexamic Acid When Used as an Adjunct to Misoprostol for the Treatment of Postpartum Hemorrhage
|
Phase 4 | |
Not yet recruiting |
NCT02853552 -
Misoprostol as First Aid Measure to Address Excessive Postpartum Bleeding
|
Phase 4 |