In Vitro Optimization of Oxytocin-induced Myometrial Contractility by Propranolol

Sponsor

Samuel Lunenfeld Research Institute, Mount Sinai Hospital (Other)

Overall Status

Recruiting

CT.gov ID

NCT03434444

Collaborator

(none)

Enrollment

Location

Arms

62.8

Anticipated Duration (Months)

0.6

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The rates of cesarean deliveries (CD) and postpartum hemorrhage (PPH) are on the rise, with failed induction and augmentation of labor as major contributing factors. Oxytocin is commonly used for labor induction, as well as during the third stage of labor to minimize the risk of primary PPH. At delivery, it is imperative that the uterus responds effectively to parenteral oxytocin. Poor response to oxytocin following delivery is commonly due to prolonged labor with oxytocin augmentation that is known to "desensitize" the myometrium. Despite the option of several second line uterotonic agents, none of them are as effective as oxytocin in controlling PPH. Given that poor uterine muscle contraction is the root cause of both failed induction or augmentation (leading to a CD in labor) and uterine atony (leading to PPH), there is an urgent and clinically important need to investigate novel methods to enhance oxytocin-induced myometrial contractions.

Propranolol, a beta adrenergic receptor agonist, has the potential to improve myometrial contractions by virtue of its ability to inhibit catecholamine production. The investigators plan to investigate the effects of propranolol in both naive and desensitized myometrium, in order to better understand its potential role in improving labor induction and reducing the risk of PPH following oxytocin exposure during labor.

The investigators hypothesize that propranolol is likely to potentiate the action of oxytocin upon human myometrium, to ultimately help improve the success of labor induction/augmentation and treatment of PPH.

Condition or Disease	Intervention/Treatment	Phase
Postpartum Hemorrhage	Drug: Oxytocin Drug: Propranolol	N/A

Detailed Description

Myometrial samples will be used to investigate the effect of propranolol on uterine contractions when exposed to high and low doses of oxytocin (to simulate PPH treatment and labor induction respectively).

The tissue will also be frozen at the end of the experiment, and Western blotting will be used to investigate the effect of propranolol on the expression patterns and cellular distribution of the oxytocin receptor and beta-adrenergic receptor and their signaling pathways in desensitized myometrium.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

40 participants

Allocation:

Non-Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

In Vitro Optimization of Oxytocin-induced Myometrial Contractility by Propranolol - Potential Applications in Induction of Labour and Treatment of Postpartum Hemorrhage

Actual Study Start Date :

Sep 8, 2017

Anticipated Primary Completion Date :

Dec 1, 2022

Anticipated Study Completion Date :

Dec 1, 2022

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: Low Dose Oxytocin The myometrial samples are bathed in an oxytocin solution at increasing concentrations (from 10 -12M to 10 -9M)	Drug: Oxytocin Oxytocin in solution, ranging from 10 -12M to 10 -5M Other Names: pitocin
Active Comparator: Propranolol The myometrial samples are bathed in a propranol solution at 10 -6M	Drug: Propranolol Propranolol in solution, 10-6M
Active Comparator: Propranolol + low dose oxytocin The myometrial samples are bathed in an oxytocin solution at increasing concentrations (from 10 -12M to 10 -9M) plus propranol (10 -6M)	Drug: Oxytocin Oxytocin in solution, ranging from 10 -12M to 10 -5M Other Names: pitocin Drug: Propranolol Propranolol in solution, 10-6M
Active Comparator: High Dose Oxytocin The myometrial samples are bathed in an oxytocin solution (10 -5M), followed by increasing concentrations of oxytocin (from 10 -8M to 10 -5M)	Drug: Oxytocin Oxytocin in solution, ranging from 10 -12M to 10 -5M Other Names: pitocin
Active Comparator: High Dose Oxytocin, Propranolol-pretreated The myometrial samples are bathed in an oxytocin solution (10 -5M) plus propranolol (10 -6M), followed by increasing concentrations of oxytocin (from 10 -8M to 10 -5M)	Drug: Oxytocin Oxytocin in solution, ranging from 10 -12M to 10 -5M Other Names: pitocin Drug: Propranolol Propranolol in solution, 10-6M
Active Comparator: High dose oxytocin + propranolol The myometrial samples are bathed in an oxytocin solution (10 -5M), followed by increasing concentrations of oxytocin (from 10 -8M to 10 -5M) plus propranolol (10 -6M)	Drug: Oxytocin Oxytocin in solution, ranging from 10 -12M to 10 -5M Other Names: pitocin Drug: Propranolol Propranolol in solution, 10-6M

Outcome Measures

Primary Outcome Measures

Motility index [3 hours]
Motility index (MI) takes into account both the amplitude and frequency of the myometrial contraction. It is a calculated outcome, based on the formula: frequency/(10 x amplitude). The analysis is undertaken by attaching myometrial strips between an isometric force transducer and the base of an organ bath chamber.

Secondary Outcome Measures

Amplitude of contraction [3 hours]
The maximum extent of uterine muscle contraction, measured in grams (g). The analysis is undertaken by attaching myometrial strips between an isometric force transducer and the base of an organ bath chamber.
Frequency of contraction [3 hours]
The number of contractions in uterine muscle (myometrium) over 10 minutes, spontaneously and in response to an agonist. The analysis is undertaken by attaching myometrial strips between an isometric force transducer and the base of an organ bath chamber.
Integrated area under response curve (AUC) [3 hours]

Eligibility Criteria

Criteria

Ages Eligible for Study:

16 Years to 40 Years

Sexes Eligible for Study:

Female

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Patients who give written consent to participate in this study
Patients with gestational age 37-41 weeks
Non-laboring patients, not exposed to exogenous oxytocin
Patients requiring primary Cesarean delivery or first repeat Cesarean delivery

Exclusion Criteria:

Patients who refuse to give written informed consent
Patients who require general anesthesia
Patients who had previous uterine surgery or more than one previous Cesarean delivery
Patients with any condition predisposing to uterine atony and postpartum hemorrhage, such as abnormal placentation, multiple gestation, preeclampsia, macrosomia, polyhydramnios, uterine fibroids, bleeding diathesis, chorioamnionitis, or a previous history of postpartum bleeding
Emergency Cesarean section in labor
Patients on medications that could affect myometrial contractility, such as nifedipine, labetolol or magnesium sulfate