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Clinical Trial Summary

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


Clinical Trial Description

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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03052686
Study type Observational
Source Centre Hospitalier René Dubos
Contact
Status Completed
Phase N/A
Start date January 2000
Completion date December 2013