common.study.topics.clinical

BMI-Associated Labor Induction: A Prospective Trial

common.study.values.description

BMI-Associated Labor Induction: A Prospective Trial

The primary objective of this study is to determine if planned induction of labor at 39 weeks for nulliparous with pre-pregnancy BMI a?Y 35 kg/m2 reduces the incidence of cesarean section compared to expectant management

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participant.ui.study.affiliations-map.online-study.header-virtual

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No pharmaceutical medication involved common.study.methods.has-drugs-no
Patients and healthy individuals accepted common.study.methods.is-healthy-no

Procedure - Labor induction

The study intervention is labor induction from 39 0/7 to 39 6/7 weeks. The individual labor induction process will be at the discretion of the physician or midwife managing the subject's care. Methods of induction that may be used include misoprostol, intracervical Foley catheter, oxytocin, and/or amniotomy. Participating clinicians will be encouraged to use only one course of cervical ripening followed by oxytocin infusion and amniotomy.

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participant.views.study.view.scientific-title

BMI-Associated Labor Induction: A Prospective Trial

common.study.values.clinical-trial-id

NCT04035382

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