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Labor Protocol Study

NCT04004845 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 66

Last updated 2022-10-04

No results posted yet for this study

Summary

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

Conditions

  • Vaginal Delivery
  • Labor
  • Induced; Birth

Interventions

DRUG

Cytotec

Misoprostol 25mcg vaginal

DRUG

oxytocin

Oxytocin 10 IU/ml Solution for infusion

DEVICE

Cervical Foley Balloon

Cervical Foley will be inflated to 80cc

Sponsors & Collaborators

  • Montefiore Medical Center

    lead OTHER

Principal Investigators

  • Peter Bernstein, MD · Montefiore Medical Center

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-03-30
Primary Completion
2022-06-01
Completion
2022-06-01
FDA Drug
Yes
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04004845 on ClinicalTrials.gov