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Clinical Trials/NCT02137200
NCT02137200TerminatedNot Applicable

Optimizing Management of the 2nd Stage of Labor: Multicenter Randomized Trial

Washington University School of Medicine6 sites in 1 country2,414 target enrollmentStarted: May 24, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
2,414
Locations
6
Primary Endpoint
Spontaneous vaginal delivery

Study Overview

Brief Summary

The investigators propose a large, multicenter, randomized clinical trial of immediate versus delayed pushing for nulliparous women in labor at term reaching complete cervical dilation. The central hypothesis is that immediate pushing in the second stage of labor increases spontaneous vaginal delivery, shortens duration of the second stage, and reduces adverse neonatal and maternal outcomes in nulliparous women. They will pursue the following specific aims: 1) Assess the effectiveness of immediate pushing at complete cervical dilation on the rate of spontaneous vaginal delivery in nulliparous women (Primary Aim), 2) Determine the effect of immediate pushing on the rate of neonatal composite morbidity (Secondary Aim #1), and 3) Determine the impact of immediate versus delayed pushing on objective and subjective measures of maternal pelvic floor morbidity (Secondary Aim #2). They estimate that randomizing a total of 3184 women will provide adequate statistical power to detect meaningful differences in the primary and secondary outcomes.

Detailed Description

A. SPECIFIC AIMS

The central hypothesis is that immediate pushing in the second stage of labor increases spontaneous vaginal delivery, shortens duration of the second stage, and reduces adverse neonatal and maternal outcomes in nulliparous women. They will pursue the following specific aims:

1) Primary Aim: Assess the effectiveness of immediate pushing at complete cervical dilation on the rate of spontaneous vaginal delivery in nulliparous women. Hypothesis: Nulliparous women will have an increase in spontaneous vaginal delivery rates with immediate, as compared to delayed, pushing.

2) Secondary Aims: i.Determine the effect of immediate pushing on the rate of neonatal composite morbidity. Hypothesis: Immediate pushing will reduce the rate of neonatal composite morbidity, defined as one or more of: neonatal death, major neonatal injury, umbilical cord arterial acidosis, suspected neonatal sepsis, respiratory distress, transient tachypnea, meconium aspiration with pulmonary hypertension, hypoxic-ischemic encephalopathy, hypoglycemia, and need for hypothermia treatment.

ii.Determine the impact of immediate versus delayed pushing on objective and subjective measures of maternal pelvic floor morbidity. Hypothesis: Immediate pushing will be associated with a reduction in the rate of acute levator ani and anal sphincter muscle injury, and lower rates of pelvic floor disorders identified on subjective and objective clinical assessments.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Singleton term pregnancy: gestational age ≥37 weeks
  • •Nulliparous women
  • •Neuraxial anesthesia: epidural or combined epidural-spinal anesthesia

Exclusion Criteria

  • •Preterm: gestational age <37 weeks (preterm infants have an a priori risk for adverse outcomes, which is driven more by gestational age than the timing of maternal pushing in the second stage)
  • •Multiple gestation (incidence of multiple gestation is small and there are unique delivery considerations)
  • •Multiparous women
  • •Non-reassuring fetal heart rate tracing (will be an indication for expedited delivery)
  • •Contraindication to vaginal delivery including: non-vertex presentation, placenta previa, prior classical cesarean, etc.
  • •No neuraxial anesthesia: epidural or combined epidural-spinal anesthesia (subjects without adequate pain control tend to push involuntarily and cannot delay pushing)
  • •Pregnancy complications requiring expedited delivery: severe preeclampsia, placental abruption, maternal cardiac disease
  • •Fetal head visible at the introitus at complete cervical dilation

Arms & Interventions

Delayed pushing

Active Comparator

Intervention: Delayed pushing (Procedure)

Immediate pushing

Experimental

Intervention: Immediate pushing (Procedure)

Outcomes

Primary Outcomes

Spontaneous vaginal delivery

Time Frame: At delivery

Spontaneous vaginal delivery will be defined as delivery that occurs without the use of forceps, vacuum, or cesarean, as the primary outcome measure.

Secondary Outcomes

  • Rate and extent of acute levator ani muscle injury(At delivery, 1 - 5 days, 4 - 8 weeks, 5 - 7 months)
  • Neonatal composite morbidity(At delivery)
  • Rates of patient-reported symptoms of urinary incontinence, fecal incontinence, and pelvic organ prolapse on physical examination(1 - 5 days, 4 - 8 weeks, and 5 - 7 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Methodius Tuuli, MD, MPH

Assistant Professor

Washington University School of Medicine

Study Sites (6)

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