NCT03024632

Brief Summary

This is a retrospective chart review. The purpose is to look at the outcomes for women and newborns who decided to attempt a trial of labor after 3 or more previous cesarean sections.

Trial Health

15
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Jan 2017

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2017

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

January 13, 2017

Completed
6 days until next milestone

First Posted

Study publicly available on registry

January 19, 2017

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2017

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2018

Completed
Last Updated

September 7, 2017

Status Verified

September 1, 2017

Enrollment Period

11 months

First QC Date

January 13, 2017

Last Update Submit

September 2, 2017

Conditions

Pregnancy

Outcome Measures

Primary Outcomes (1)

  • Number of Vaginal births

    outcomes and safety of a trial of labor after 3 or more previous c-sections managed at a tertiary care facility

    Labor through 6 weeks postpartum

Study Arms (2)

trial of labor

Pregnant women with a history of 3 or more cesarean sections who desired a trial of labor

Procedure: Trial of labor

No trial of labor

Pregnant women with a history of 3 or more cesarean sections who desired a a repeat cesarean section

Interventions

Trial of laborPROCEDURE

trial of labor after 3 or more previous cesarean deliveries

trial of labor

Eligibility Criteria

Age14 Years - 55 Years
Sexfemale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

14-55yrs of age Pregnant all ethnic backgrounds

You may qualify if:

  • Women with a history of 3 or more cesarean sections
  • pregnant
  • singleton

You may not qualify if:

  • Less than 3 cesarean sections

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Trial of Labor

Intervention Hierarchy (Ancestors)

Labor, ObstetricPregnancyReproductionReproductive Physiological PhenomenaReproductive and Urinary Physiological Phenomena

Study Officials

  • Christopher Q Buchanan, MD

    St. Louis University

    STUDY DIRECTOR
0

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

January 13, 2017

First Posted

January 19, 2017

Study Start

January 1, 2017

Primary Completion

December 1, 2017

Study Completion

June 1, 2018

Last Updated

September 7, 2017

Record last verified: 2017-09

Data Sharing

IPD Sharing
Will not share