Optimization of Routine Obstetric and Neonatal Care in the Management of Severe Perinatal Asphyxia in Term or Near-term Newborns: Analysis of Sub-optimal Care

Recruiting Observational Study
Perinatal Asphyxia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
Up to 1 Month
Sex
Any
Study type
Observational
Participants needed
336 (estimated)
Sponsor
Assistance Publique - Hôpitaux de Paris · Other
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About This Trial
The purpose of this study is to identify and analyze suboptimal perinatal (obstetric-pediatric) care in the occurrence and management of severe perinatal asphyxia or death of the newborn at or near term. Perinatal asphyxia is a serious and often unexpected pathology, requiring urgent multidisciplinary care (obstetric - pediatric - intensive care, etc.) with a high level of technical expertise and…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: \- Newborn at or near term (≥ 36 weeks of amenorrhea), considered to be alive at the onset of labor and presenting severe perinatal asphyxia Severe perinatal asphyxia is considered if 1. Severity in its impact on the newborn: • a neonatal death during the initial hospitali…
Contacts

Pierre DELORME, MD, PhD

01 44 73 51 20

pierre.delorme@aphp.fr

CONTACT

Valérie PLENCE, PHD

01 58 41 11 78

valerie.plence-fauroux@aphp.fr

CONTACT