Labor Protocol Study

Status Terminated

Clinical Trial Summary

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

Clinical Trial Description

This is quasi-experimental prospective cohort study with historical control to examine the efficacy of a new labor induction bundle. The prospective cohort will consist of all eligible nulliparous and multiparous patients admitted for induction; the historical control group will consist of all eligible nulliparous and multiparous patients admitted for induction between August 2019 and February 2020. Patients who are part of the prospective cohort who do not consent to the labor bundle due to personal or physician preferences will be included in secondary analyses as a contemporary control group, however the sample size of this group will not be determined in advance. Objective: To assess if implementation of an evidence-based labor induction bundle will increase the rate of vaginal delivery within 24 hours. Hypothesis: Implementation of a labor induction bundle would result in a 30% increase in the rate of vaginal delivery within 24 hours. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04004845
Study type	Observational
Source	Montefiore Medical Center
Contact
Status	Terminated
Phase
Start date	March 30, 2021
Completion date	June 1, 2022

View Details

See also
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