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Head-perineum Distance and Delivery Mode

Correlation Between Head Perineum Distance Measured by Trans-périneal Ultrasound and Delivery Mode in Patient in the Second Stage of Labor

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04771091
Acronym
EchoPé
Enrollment
280
Registered
2021-02-25
Start date
2020-07-08
Completion date
2021-04-04
Last updated
2023-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obstetric Labor, Pregnancies

Keywords

Head perineum distance, ultrasound measure, delivery mode, instrumental delivery, spontaneous delivery, pushing maternal efforts

Brief summary

In a prospective cohort of patients in the second phase of labor, the investigators measured the head-perineum distance and correlate it to the mode of delivery (spontaneous delivery - instrumental delivery - ceasarean section).

Detailed description

Head-perineum distance measured by transperineal ultrasound is a simple and well-known tool to help diagnose the fetal head engagement and predictive value to instrumental extraction succeeds. It is performed in labor room and is a non-invasive test, realized on a healthy skin. The investigators performed a systematical measure of head perineum distance at the beginning of the expulsive labor phase. The investigators made the hypothesis, based on our clinical experience, that starting expulsive labor phase with head perineum distance greater than forty five millimeters, lead to an increased risk of instrumental extraction and therefore an increase in materno-fetal morbidity and mortality. The investigators sought to evaluate the optimal head perineum distance at the beginning of expulsive efforts.

Interventions

DIAGNOSTIC_TESTMesure of head-perineum distance by transperineal ultrasound

A mesure of head-perineum distance by ultrasound will be realized at the beginning of maternal pushing efforts by a junior gynecologist

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Single pregnancy * In labor (spontaneous or induced) * Term superior at 37 SA * Delivery by summit presentation

Exclusion criteria

* Non single pregnancy * Suspected malformative abnormalities in the unborn fetus * Refusal of participation * Minor patient * Adult patient subject to legal protection or patient deprived of liberty * Poor French language understanding

Design outcomes

Primary

MeasureTime frameDescription
Delivery modeDay 1spontaneous or instrumental vaginal delivery

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026