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Clinical Trial Summary

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


Clinical Trial Description

Obesity in the obstetric population has reached epidemic proportions, affecting over 30% of reproductive-aged women in the United States (1). The increase in this morbidity is associated with large increases in cesarean delivery over the non-obese obstetric population and resultant post-operative complications are also higher in obese women (2). There are no interventions proven to reduce the risk of cesarean in obese women. The aim of this research study is to determine if induction of labor at 39 weeks can reduce the incidence of cesarean delivery over routine obstetric care (expectant management). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04035382
Study type Interventional
Source Baystate Medical Center
Contact Corina Schoen, MD
Phone 413-794-3470
Email Corina.SchoenMD@baystatehealth.org
Status Recruiting
Phase N/A
Start date October 31, 2019
Completion date December 31, 2022

See also
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