NCT07071662

Brief Summary

Breech presenting fœtus were generally not offered a trial labor induction and were instead directed toward a cesarean section. This approach often led to obstetric complications for both the mother and the fetus. This study aims to offer more labor inductions to patients with a fetus in breech presentation in order to avoid the mobidity and mortality associated with systematic cesarean sections.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
102

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jun 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

June 30, 2025

Completed
8 days until next milestone

First Submitted

Initial submission to the registry

July 8, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

July 17, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2025

Completed
Last Updated

March 27, 2026

Status Verified

March 1, 2026

Enrollment Period

3 months

First QC Date

July 8, 2025

Last Update Submit

March 26, 2026

Conditions

FailureBreech Presentation at TermLabor Induction at Term

Keywords

labor inductionfailurebreech presentation

Outcome Measures

Primary Outcomes (2)

  • number of vaginal delivery

    day 1

  • Number of cesarean

    day 1

Secondary Outcomes (4)

  • number of Endometrite

    day 1

  • lactates value

    day 1

  • Apgar value

    day 1

  • Number of neonatology admission

    day 1

Study Arms (2)

vaginal delivery

Other: delivery mode

caesarean

Other: delivery mode

Interventions

delivery modeOTHER

To observe the different modes of delivery and evaluate the characteristics of the patients as well as maternal and fetal well being in the post partum period.

caesareanvaginal delivery

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailspregnant women
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patients with a fetus in breech presentation

You may qualify if:

  • singleton
  • consent for vaginal delivery
  • breech presenting

You may not qualify if:

  • minor
  • twin pregnancy
  • refusal of vaginal delivery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHRU Amiens

Amiens, 80480, France

Location

MeSH Terms

Conditions

Breech Presentation

Condition Hierarchy (Ancestors)

Obstetric Labor ComplicationsPregnancy ComplicationsFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital Diseases

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 8, 2025

First Posted

July 17, 2025

Study Start

June 30, 2025

Primary Completion

October 1, 2025

Study Completion

October 1, 2025

Last Updated

March 27, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations

FR(1)