Retrospective Study of 110 Cases of Uterine Rupture to Determine Obstetric and Neonatal Complications

NCT03052686 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 110

Last updated 2017-02-14

No results posted yet for this study

Summary

This study has for objective to collect medical data from patients with uterine rupture at the childbirth.

Conditions

  • Anomaly Uterus

Interventions

OTHER

Childbirth with uterine rupture

No intervention. Follow-up of women with rupture uterine at the childbirth.

Sponsors & Collaborators

  • Hôpital NOVO

    lead OTHER

Principal Investigators

  • MARKOU Georges, PH · CH Rene Dubos, Pontoise

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2000-01-31
Primary Completion
2013-12-31
Completion
2013-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03052686 on ClinicalTrials.gov