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In-vitro Myometrial Contractility After Oxytocin Pre-exposure in Women With Advanced Maternal Age and Morbid Obesity

In-vitro Myometrial Contractility After Oxytocin Pre-exposure in Women With Advanced Maternal Age and Morbid Obesity

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01865669
Enrollment
44
Registered
2013-05-31
Start date
2013-05-31
Completion date
2017-06-13
Last updated
2018-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum Hemorrhage

Keywords

Uterine contraction, Dose response, Oxytocin

Brief summary

Women with advanced maternal age and morbid obesity, have a higher incidence of labor induction/ augmentation and cesarean section (CS), and are at a greater risk for postpartum hemorrhage (PPH). Oxytocin is the first line drug in the treatment of PPH, however, oxytocin receptor (OTR) desensitization has been recognized in the context of prolonged labors secondary to either endogenous or exogenous oxytocin exposure. It is unknown if oxytocin desensitization specifically affects contractility in women with advanced maternal age and morbid obesity when compared to younger or normal weight populations. Further it is not known if the higher incidence of PPH seen in these women is due to poor uterine contractility and/or poor response to oxytocin. The investigators hypothesize that women with advanced maternal age and morbid obesity will exhibit poor myometrial contractility as compared to women that are younger and of normal body habitus, in both oxytocin pre-treated and untreated myometrium.

Detailed description

In view of the growing concern over the rising incidence of later maternal age and morbid obesity in the obstetric population, scientific evidence on pregnancy outcomes in these patients is timely and important. The investigators' previously validated in-vitro model provides a solid foundation for the study of myometrial contractility under controlled conditions, without any confounders that could be encountered in clinical settings. It is also likely to provide in-depth understanding of the parameters that the investigators feel are responsible for higher incidence of PPH in these patients. The investigators' study will form a basis for future modifications in oxytocin augmentation regimens and pharmacotherapy for control of PPH in these patient populations.

Interventions

DRUGOxytocin

Oxytocin, 10-10mol/L to 10-5mol/L

Sponsors

Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* patients who give written informed consent * patients requiring elective primary or 1st repeat Cesarean section * patients with gestational age 37-41 weeks * non-labouring patients, not exposed to exogenous oxytocin * Cesarean section under spinal anesthetic * patients \<30 years of age with a normal pre-pregnancy BMI (20 and 24.9 kg/m2) * patients ≥40 years of age with a normal pre-pregnancy BMI * patients with a BMI≥40 kg/m2 and age \<30 years

Exclusion criteria

* patients who refuse to give written informed consent * patients who require general anesthesia * patients who have had more than one previous uterine surgery/CS * patients with placental abnormalities (abruption, accreta, percreta) * patients with bleeding disorders * presence of any other risk factors for PPH

Design outcomes

Primary

MeasureTime frame
Motility index6-8 hours

Secondary

MeasureTime frame
Amplitude of contraction6-8 hours
Integrated area under response curve (AUC)6-8 hours
Frequency of contraction6-8 hours

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026