Actively Recruiting
Prognosis of Patients Who Presented With a State of Extreme Agitation.
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-04-04
608
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
Sponsors
A
Assistance Publique - Hôpitaux de Paris
Lead Sponsor
L
Lariboisière-Saint Louis clinical research unit
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Prognosis of Patients Who Presented With a State of Extreme Agitation.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- patient age < 18 years
- head trauma
- pregnancy
- detained
- other obvious causes of pain leading to restlessness (renal colic, migraines, etc.)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Avicenne Hospital - Aphp
Bobigny, Île-de-France Region, France, 93000
Actively Recruiting
Research Team
F
Frédéric Adnet, MD, PhD
CONTACT
E
Eric Vicaut, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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