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Assessment of the pelvic centre in MRI pelvimetry as a predictive value for successful vaginal delivery.

Assessment of the pelvic centre in MRI pelvimetry as a predictive value for successful vaginal delivery.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00031376
Enrollment
350
Registered
2023-02-27
Start date
2021-10-09
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Breech presentation, cephalopelvic disproportion O32

Interventions

Group 1: Retrospective analysis of all patients who received MRI_pelvimetry during pregnancy between 02/2001 and 06/2021 as part of routine care at the Großhadern Perinatal Centre.

Sponsors

Klinik und Poliklinik für Frauenheilkunde und Geburtshilfe Campus Großhadern, Ludwig-Maximilians-Universität München
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: All data sets of patients included in the study who received MRI pelvimetry during pregnancy between 02/2001 and 06/2021 as part of routine care at the Großhadern Perinatal Centre. Inclusion criteria: Presence of MRI pelvimetry in the course of pregnancy. Presence of the birth protocol

Exclusion criteria

Exclusion criteria: Incomplete data set (Lost to follow up)

Design outcomes

Primary

MeasureTime frame
Primary objective: Do the measurements of the pelvic centre and the shape of the sacral cavity correlate with a successful vaginal birth?

Secondary

MeasureTime frame
Secondary objectives: o Child outcome o Rate of vaginal operative births o Rate of secondary sectiones o Duration of the expulsion period o Impaired child development in the event of a secondary section o Maternal outcome

Countries

Germany

Contacts

Public ContactUwe Hasbargen

Klinik und Poliklinik für Frauenheilkunde und Geburtshilfe Campus Großhadern, Ludwig-Maximilians-Universität München

uwe.hasbargen@med.uni-muenchen.de+49 89 4400 74540

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026