TerminatedNot Applicable

Labor Protocol Study

Stopped: Study was temporarily paused due to COVID19 and ultimately terminated at the discretion of the PI

United States66 participantsStarted 2021-03-30

Plain-language summary

The goal of this study is to see if there is a better way to induce labor.

Age range18 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

✓. Singleton pregnancy
✓. Cephalic presentation
✓. Gestational age 36 weeks 6 days- 42 weeks 0 days at initiation of induction of labor
✓. Age 18 and over

✕. Preterm (less than 36 weeks 6 days) at initiation of induction of labor
✕. Non-cephalic presentation
✕. Major fetal anomalies or intrauterine fetal death
✕. Bishop score more than 6 at initiation of induction of labor
✕. Any contraindication to any agents in the induction protocol (i.e. prior cesarean delivery or myomectomy, three or more contractions per ten minute period averaged over 30 minutes at the initiation of induction of labor, low lying placenta).
✕. Any contraindication to vaginal delivery
✕. Latex allergic

Percentage of Vaginal Deliveries

Timeframe: Within 24 hours

NCT IDNCT04004845

SponsorMontefiore Medical Center

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2022-06-01