Informations générales (source: ClinicalTrials.gov)
Prospective Cohort of Severe Trauma Patients Hospitalized in West French Intensive Care Units
Observational
Nantes University Hospital (Voir sur ClinicalTrials)
mars 2013
janvier 2050
29 juin 2024
The purpose of this observational epidemiological study is to investigate the management
and the complications associated with severe trauma. Data will be analysed to answer
pre-defined scientific projects and to improve management of these conditions.
Etablissements
Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
---|---|---|---|---|---|
Angers University Hospital - 49000 - Angers - France | Sigismond LASOCKI, PhD, MD | Contact (sur clinicalTrials) | |||
Nantes University Hospital - 44093 - Nantes - France | Contact (sur clinicalTrials) | ||||
Rennes University Hospital - 35000 - Rennes - France | Yannick MALLEDANT, PhD, MD | Contact (sur clinicalTrials) | |||
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
Poitiers University Hospital - 86000 - Poitiers - France | Olivier MIMOZ, PhD, MD | Contact (sur clinicalTrials) | |||
Tours University Hospital - 37000 - Tours - France | Martine FERRANDIERE, MD | Contact (sur clinicalTrials) |
Critères
Tous
Inclusion Criteria:
- severe trauma
- and/or traumatic brain injury
- and/or hemorrhage
- severe trauma
- and/or traumatic brain injury
- and/or hemorrhage
- Consent withdrawal