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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

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.

Eligibility criteria

Qualifiers

Agitated patient with the presence of three major criteria, namely,

restlessness

insensitivity to pain

tachypnea (fr>20)

Disqualifiers

patient age < 18 years

head trauma

pregnancy

detained

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Sponsors and collaborators

Assistance Publique - Hôpitaux de Paris

Lead sponsor

Lariboisière-Saint Louis clinical research unit

Collaborator