About this trial
This pilot, randomized control trial will test whether or not a specific circuit of position changes improves maternal outcomes in cases of prolonged labor.
Patient who have prolonged labor will be approached for consent and randomization to one of two study groups: circuit intervention against routine standard of care position changes. 82 patients will be enrolled in the study. Exclusion criteria will include: any uterine infection prior to randomization, magnesium sulfate treatment, major fetal anomalies, BMI ≥50, non-reassuring fetal status prior to randomization, or any maternal diagnosis that precludes safety or feasibility of the circuit of maternal position changes.
The 3 aims of the study will include: the outcome that the circuit of position changes has on the duration of the first stage of labor, maternal and neonatal morbidity, and maternal satisfaction.
Eligibility criteria
Qualifiers
English-speaking patients
Singleton, vertex pregnancies
34 weeks' gestation or later
Admitted to Labor and Delivery in spontaneous labor or for an induction of labor
Disqualifiers
Intraamniotic infection prior to randomization
Magnesium sulfate treatment
Major fetal anomalies
BMI ≥50
Trial design
Treatments tested in this trial
- Circuit of maternal position changes during labor
Treatment groups
Locations
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Sponsors and collaborators
Washington University School of Medicine
Lead sponsor
Barnes-Jewish Hospital
Sponsor institution
Barnes-Jewish Hospital
Collaborator
The Foundation for Barnes-Jewish Hospital
Collaborator