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Prognosis of Patients Who Presented With a State of Extreme Agitation.

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.

Condition(s)Emergence Delirium
StatusRecruiting
Study typeObservational
SummaryThe 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.
Who can participateInclusion Criteria: * Agitated patient with the presence of three major criteria, namely, * restlessness * insensitivity to pain * tachypnea (fr\>20) and the presence of a minor criterion among * sweating * skin hyperthermia * non-compliance with law enforcement * tirelessness * unusual strength * inappropriate clothing, nudity Exclusion Criteria: * patient age \< 18 years * head trauma * pregnancy * detained * other obvious causes of pain leading to restlessness (renal colic, migraines, etc.)
Ages18 Years
SexAll
Lead sponsorAssistance Publique - Hôpitaux de Paris
LocationsBobigny, Île-de-France Region, France
Start date2023-01-17
NCT IDNCT05632419
Official listinghttps://clinicaltrials.gov/study/NCT05632419

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