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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04153331
Other study ID # 69HCL19_0755
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 13, 2020
Est. completion date March 9, 2020

Study information

Verified date January 2020
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Seasonal influenza surveillance in France relies on several sources to detect the onset of the epidemic early, as well as to estimate the severity of epidemics and their impact on the health system. However, the data collected do not fully measure the impact of epidemics on the hospital system.

Increasing the investigator's knowledge of the impact of influenza on the hospital system, particularly on emergencies, which are the most affected service, is essential to better adapt the resources put in place to care for patients.

The study will allow a better understanding of the influenza burden, by systematically documenting the severe events (i.e. requiring consultations to the Emergency Rooms) that are triggered by influenza but not necessarily reported/recorded as influenza.


Recruitment information / eligibility

Status Completed
Enrollment 2487
Est. completion date March 9, 2020
Est. primary completion date March 9, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age > 18 years

- Consultation for a medical cause

Exclusion Criteria:

- Consultation for a non-medical cause (trauma...)

- Pregnant, parturient and lactating women

- Persons deprived of their liberty

- Persons of full age who are subject to a legal protection measure

- Persons not affiliated to a social security system

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Nasal swab
Patient included in emergency with a nasal swab

Locations

Country Name City State
France Service Hygiène, Epidémiologie et Prévention Lyon

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 Proportion of laboratory confirmed influenza among patients admitted to Emergency Room during the influenza season The proportion of laboratory confirmed influenza cases will be calculated by dividing the number of patients with laboratory confirmed influenza by the total number of patients included 1 day (at admission)
Secondary Proportion of patients with co-morbidities to evaluate the proportion of patients consulting emergency department who have co-morbidities according to the result of the virological sampling 1 day (at admission)
Secondary Proportion of patients with laboratory confirmed influenza and related outcomes to estimate the proportion of patients with a laboratory confirmed influenza stratified on the emergency department visit outcomes (hospitalization in medicine, hospitalization in intensive care unit or return home) and other covariates 1 day (at admission)
Secondary Proportion of patients who consult for other causes than influenza to estimate the proportion of patients with a laboratory confirmed influenza consulting for other causes than influenza 1 day (at admission)
Secondary Proportion of asymptomatic influenza cases among patients with laboratory confirmed influenza The proportion asymptomatic influenza cases will be calculated by dividing the number of patients with asymptomatic influenza by the total number of laboratory confirmed influenza 1 day (at admission)
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