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Clinical Trial Summary

The main objective is to assess the 6-month prognosis of patients who presented with extreme agitation in the emergency room. The primary endpoint is the 6-month mortality of agitated patients.


Clinical Trial Description

Emergency services are confronted with emergency situations characterized by patients who are victims of significant agitation, in particular states of extreme agitation "excited delirium syndrome", which is constantly increasing and which seems to be associated with morbidity and mortality not negligible. Patients meeting the inclusion and non-inclusion criteria are included on admission to the emergency room. An evaluation at H1 and at the end of hospitalization is carried out. The patient is contacted by telephone at M1, M3 and M6. The inclusion period is 24 months The duration of participation (treatment + follow-up) is 6 months The total duration is 30 months. The research is multicentric and national with the participation of 8 centres. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05632419
Study type Observational
Source Assistance Publique - Hôpitaux de Paris
Contact Frédéric Adnet, MD, PhD
Phone 01 48 96 44 08
Email frederic.adnet@avc.aphp.fr
Status Recruiting
Phase
Start date January 17, 2023
Completion date January 17, 2025

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