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Study of the Value of Maternal-fetal Transfers and Their Complexity of Their Implementation

Study of the Value of Maternal-fetal Transfers and Their Complexity of Their Implementation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06480916
Acronym
TRANSFERT
Enrollment
101
Registered
2024-06-28
Start date
2024-04-01
Completion date
2025-04-01
Last updated
2026-06-24

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

Conditions

Maternal-Fetal Relations

Keywords

maternal-fetal transfer, care organization, patient pathway, maternity hospital

Brief summary

It is an observational, descriptive, prospective, multicenter study of 8 maternity units in Lorraine and Champagne-Ardenne, aimed at comparing the percentage of "avoidable" maternal-fetal transfers (MFTs), defined as transfers in which the delivery finally meets the acceptance criteria of the sending maternity unit, according to the obstetrical indications for these MFTs.

Detailed description

Over the past year, an audit carried out on the Mercy maternity unit, covering 130 transfers to the Nancy regional maternity hospital, showed that patients transferred for threat of premature delivery (MAP) with a cervix \> 15 mm do not give birth at the receiving maternity unit, but return home after 48 hours' hospitalization. When maternal-fetal transfer (MFT) is requested, numerous calls are made to private ambulance services, and in the end, many emergency rapid response units (SMUR) are called out, requiring a major human, logistical and time investment for a questionable benefit to the patient. Tensions in terms of logistics (lack of ambulance, SMUR) and human resources (lack of personnel) can, conversely, compromise good care of the parturient.

Interventions

PROCEDUREMaternal-fetal transfers

Prospective and consecutive inclusion of all maternal-fetal transfers during the study period. The teams at the sending and receiving maternity units will complete study-related questionnaires to describe the conditions of the transfer and the outcome of the pregnancy. The study in no way alters the way parturients are cared for.

Sponsors

Centre Hospitalier Régional Metz-Thionville
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* Pregnant woman cared for in a participating maternity unit * Over 18 years of age * Requested for maternal-fetal transfer (finally performed, or not)

Exclusion criteria

* missing data on transfer outcome

Design outcomes

Primary

MeasureTime frameDescription
The percentage of "avoidable" maternal-foetal transfer (MFT)after delivery, up to 6 weeks after the maternal-foetal transferThe main evaluation criterion is "avoidable" maternal-foetal transfer (MFT), i.e. resulting in a delivery that met the acceptance criteria of the original maternity hospital

Secondary

MeasureTime frameDescription
Obstetrical indication for maternal-foetal transfer (MFT)Up to 48 hours after the maternal-foetal transferas documented in the patient file
Organizational arrangements for maternal-foetal transferUp to 6 months after inclusion of a maternity unit in the studyOrganizational arrangements for maternal-foetal transfer in the various centers, assessed by a specific questionnaire sent to maternity units.

Countries

France

Contacts

PRINCIPAL_INVESTIGATORLaetitia HONORE-ROUGE, MD

CHR Metz Thionville Hopital Femme Mère Enfant

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 25, 2026