Prognosis of Patients Who Presented With a State of Extreme Agitation.
ConditionEmergence Delirium
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
This trial does not accept healthy volunteersQualifiers
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 population
Agitated patients
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Number of deceased patients
The 6-month prognosis of patients who presented with extreme agitation in the emergency room.
Time frame
6 monthsSecondary outcomes
1
Assess the characteristics of agitated patients regarding the age
Age
Time frame
6 months2
Assess the characteristics of agitated patients regarding the gender
Gender
Time frame
6 months3
Assess the characteristics of agitated patients regarding the mode of arrival in the emergency room
Mode of arrival in the emergency room
Time frame
6 months4
Assess the characteristics of agitated patients regarding medical history
Medical history
Time frame
6 monthsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Assistance Publique - Hôpitaux de Paris
Lead sponsor
Lariboisière-Saint Louis clinical research unit
Collaborator
Source ClinicalTrials.gov