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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04726449
Other study ID # 69HCL20_1071
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 11, 2021
Est. completion date May 8, 2024

Study information

Verified date July 2023
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Use of emergency department for psychiatric symptoms always addresses the question of a potential somatic cause to the symptoms. Despite the wide-spread use of standard biology test and systematic brain imaging (for a first episode), there are still up to 5% of patients sent in psychiatric wards that actually have a somatic explanation to their symptoms which induces an important delay in the diagnostic assessement We hypothesized that simple neurological clinical examination along with fast psychometric screening tests in the Emergency Room (ER) could help the physicians to better screen the patients and thus prevent inaccurate post-emergency orientation. Every patient visiting the ER for psychiatric symptoms will be included. The usual physical examination by the ER physician will be associated with two psychometric tests (namely the Clock-drawing test and Frontal Assessment Battery test). The follow up will be made after 3 months in order to have the final diagnosis. Neurological data and data from the FAB test and the Clock-drawing test will be compared between patients who were finally given a psychiatric diagnosis versus patients with a somatic diagnosis at the end of the follow up period.


Recruitment information / eligibility

Status Completed
Enrollment 148
Est. completion date May 8, 2024
Est. primary completion date May 8, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age> 18 years old - Patient consulting the emergency room for psychiatric recourse - Benefiting from a consultation with a psychiatrist in the emergency room - Patient affiliated to a social security scheme Exclusion Criteria: - Pregnant or breastfeeding women - Patient objecting to the conduct of this study and the collection of health data - Patient with motor disorders preventing the performance of a test requiring a pencil - Patient sedated before treatment in the emergency room - Patient with visual disturbances

Study Design


Intervention

Other:
Screening for acute confusional state
The intervention will consist of two psychometric test to screen for acute confusional state with the usual physical examination by the emergency physician. The neurological examination abnormalities will be noted

Locations

Country Name City State
France Service Accueil des Urgences, Hopital Edouard Herriot Lyon Rhône

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Somatic or psychiatric nature of the final diagnosis given to the patient interview patient to collect during the last 90 days the data of a hospitalization, its possible duration, the examinations that may have been necessary to obtain the diagnosis: blood, urine, Cerebrospinal Fluid, imaging exams, electroencephalography. At 3 month
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