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Completed

NCT Number: NCT03052686

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

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

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Key information

Conditions

Anomaly Uterus Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Genital Diseases Genital Diseases, Female Obstetric Labor Complications Pregnancy Complications Rupture Urogenital Diseases Uterine Anomalies Uterine Diseases Uterine Rupture Wounds and Injuries

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Hôpital NOVO

Cergy-Pontoise, 95300, France

About this study

This is a retrospective study, gathering data of five maternity in the department of Val d'Oise in France, during 13 years (between 01/01/2000 an 31/12/2013).

The incidence of uterine rupture increases with increasing cesarean rates. It occurs at a rate of 0.08% across all childbirths in France, and 0.5 to 1% of the childbirths on cicatricial uterus in France.

Although the risk factors are known, it is usually unexpected. This is a serious complication for the mother (mortality <1%, severe morbidity at 15% ) and for the child (mortality for 3 to 6 % for childbirth at term, neonatal asphyxia for 6 to 15%) that can occur during pregnancy or during labor.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Childbirth with uterine rupture

Exclusion criteria

  • Childbirth in a maternity which do not participate to the study

Treatment and study plan

Childbirth with uterine rupture

Other

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

Primary outcomes

  1. Identify maternal and foetal risk factors associated to an uterine rupture ; by the report of events during pregnancy, pathology, lifestyle, Concomitant pathology...

    Time frame: 1 day

Secondary outcomes

  1. Number of maternal and foetal adverse events associated to an uterine rupture at the childbirth.

    Time frame: 1 day

Sponsors and collaborators

Lead sponsor

Hôpital NOVO

Other

Registry information

Acronym: RUVO

Important dates

Study start
2000
Primary completion
2013
Study completion
2013
First posted
Feb 14, 2017
Registry last updated
Jun 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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