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Obstetrical Outcomes for Planned Deliveries in a French Birth Center

Obstetrical Outcomes for Planned Deliveries in a French Birth Center

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05845879
Acronym
NidaModa
Enrollment
200
Registered
2023-05-06
Start date
2023-06-01
Completion date
2024-05-01
Last updated
2023-05-23

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

Conditions

Delivery Complication

Brief summary

The main objective of this work is to study the obstetrical and neonatal outcomes of women who planned to deliver in the birth centre of Nancy. The birth centre of Nancy is one of the nine french birth centres opened since 2015 on an experimental basis. The women who plan to deliver at the birth centre must meet several conditions according to their medical history, pregnancy follow-up, and delivery progress. The women can be transferred before, during or after (pre-, per- or post-) delivery to the hospital.

Interventions

OTHERdelivery

delivery

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
19 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* women who want to deliver at the birth center Un nid pour naître

Exclusion criteria

* Refusal to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
Comparison of the cesarean birth rate of women who planned to deliver in the birth centre according to the final place of labor (hospital or birth centre).4 yearsrate of cesarean section
Comparison of the instrumental birth rate of women who planned to deliver in the birth centre according to the final place of labor (hospital or birth centre).4 yearsrate of instrumental birth (vacuum or forceps delivery)
Comparison of the post-partum haemorrhage rate of women who planned to deliver in the birth centre according to the final place of labor (hospital or birth centre).4 yearsrate of post-partum haemorrhage define by blood loss \>= 500 cc

Secondary

MeasureTime frameDescription
Comparison of the antepartum or peripartum stillbirth rate of women who planned to deliver in the birth center according to the final place of labor (hospital or birth centre).4 years
Comparison of the umbilical artery blood pH score of babies from women who planned to deliver in the birth centre according to the final place of labor (hospital or birth centre).4 years
Comparison of the hypoxemic encephalopathy rate of women who planned to deliver in the birth center according to the final place of labor (hospital or birth centre).4 years
Comparison of the five-minute Apgar score of babies from women who planned to deliver in the birth centre according to the final place of labor (hospital or birth centre).4 yearsApgar score is a score that records the physical condition of a baby just after it is born, with ten points being the highest possible score and zero point the lowest.

Outcome results

None listed

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