Labor Dystocia, Labour;Obstructed
Conditions
Brief summary
Induction of labor is one of the most common procedures performed on labor and delivery. In the United States, more than 20 percent of pregnant women undergo an induction of labor \[1\]. There is data from small, randomized studies that demonstrates the effectiveness of propranolol, a non-selective beta-blocker, for labor augmentation. This literature suggests a decrease in the amount of time to delivery and a possible reduction in cesarean section rates when propranolol is used in conjunction with oxytocin for induction of labor compared to oxytocin alone \[2-8\]. Alpha- and beta-adrenergic receptors have been identified in the human myometrium. Propranolol has been shown in studies to enhance uterine contractions and may be a useful tool in this population of women. Therefore, the purpose of this study is to assess whether the administration of propranolol at time of labor dystocia reduces time to delivery.
Detailed description
All cervical ripening will be performed in the labor and delivery unit; continuous fetal heart rate and uterine activity will be monitored in all patients. Cervical dilation is assigned by admitting physicians. Sonography will be performed to document fetal presentation. At the time of prolonged labor, patients meeting inclusion criteria and no exclusion criteria will be consented. There will be no monetary incentives for participation. Patients will be randomized to either Propranolol 2mg of IV or expectant management at the time of induction. Maternal vitals will be collected per standard labor management. Episodes of uterine activity that are deemed excessive by the physician will be treated with a standard combination of maneuvers that included a change in maternal position, oxygen administration, and terbutaline 250 µg subcutaneously. Persistent abnormal fetal heart rate patterns resulted in intervention by removing the patient from the study. Urgent cesarean delivery is defined as a cesarean delivery performed during the ripening process for abnormal fetal heart rate that did not respond to standard maneuvers.
Interventions
DRUGPropranolol
Propranolol 2mg IV
Sponsors
Christiana Care Health Services
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* ≥18 years of age * full term (≥37 weeks) gestations determined by routine obstetrical guidelines * singleton gestation in cephalic presentation * Intact membranes * Bishop score of ≤6 and cervical dilation ≤2cm
Exclusion criteria
* Preterm gestation * Diabetes requiring insulin in labor: given the potential risk of neonatal hypoglycemia in the neonate * multiparous women * Any cardiac condition for which β blockade is contraindicated (cardiogenic shock, sinus bradycardia, and greater than first degree heart block) * Known hypersensitivity to propranolol * Maternal bradycardia (HR \<60bpm) * Severe preeclampsia: as patients will be receiving magnesium and possibly labetalol for hypertension control * Systolic blood pressure \<90 mmHg, or diastolic blood pressure \<50 mmHg * Receiving other beta blocker * Moderate or severe asthma: as this is a contraindication to beta blocker use * Any contraindication to a vaginal delivery * fetal demise * Multifetal gestation * major fetal anomaly * prior uterine surgery, previous cesarean section * women with HIV, hepatitis C, hepatitis B, and women with medical conditions requiring an assisted second stage * Additional
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| time to delivery | Number of hours from induction to delivery of neonate; up to 72 hours. | The primary outcome is time to delivery (hours) defined as time from initiation of induction method to delivery time, regardless of mode of delivery. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| maternal length of stay | From time of admission to time of hospital discharge; an average of two days | from time of admission to discharge |
| Maternal Bradycardia event | at time of delivery | bradycardia alert during labor |
| Chorioamnionitis | At time of delivery | defined by the presence of maternal fever ≥100·4°f in the presence of maternal or fetal tachycardia or fundal tenderness |
| neonatal admission to ICU | At time of delivery | NICU admission |
| cesarean delivery rate | At time of delivery | rate of cesarean delivery |
| neonatal sepsis | at time of delivery | Culture proven-presumed neonatal sepsis |
| Neonatal blood transfusion | From time of delivery to time of hospital discharge; up to 6 weeks | Neonatal blood transfusion |
| Hypoxic ischemic encephalopathy | through study completion, an average of 1 year | neonatal HIE |
| Severe respiratory distress syndrome | at time of delivery | defined as intubation and mechanical ventilation for a minimum of 12 hours |
Countries
United States
Outcome results
None listed