Nosocomial Influenza Surveillance 2018 - 2022
NOSOGRIPPE
Surveillance of Nosocomial Influenza at Edouard Herriot University Hospital, Lyon, France.
1 other identifier
observational
500
1 country
1
Brief Summary
Hospital-acquired influenza is associated with significant morbidity and mortality in hospitalized patients notably elderly patients. Furthermore, it is also associated with a large economic impact for the hospitals. The transmission of influenza has been mostly reported in pediatric and long-stay units. The chains of transmission of influenza in acute-stay units have to be describe in order to prevent and control potential outbreaks. Furthermore, to know clinical symptoms seems to be important in order to identify potential sources of virus as soon as possible and to set up appropriate hygiene prevention measures. Moreover, the definition of the hospital-acquired influenza has to be harmonized for all over the studies, especially concerning the delay between the admission in the hospital and the symptoms onset. The aim of this study is to describe the hospital-acquired influenza in a french university hospital of around 800 beds
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2018
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 22, 2018
CompletedFirst Posted
Study publicly available on registry
January 29, 2018
CompletedStudy Start
First participant enrolled
February 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2022
CompletedJanuary 30, 2018
January 1, 2018
4 months
January 22, 2018
January 26, 2018
Conditions
Outcome Measures
Primary Outcomes (1)
Proportion of patients and health-care workers who present an influenza illness.
An interview to collect some informations will be done to evaluate if participants present symptoms of an inflenza illness (fever \> 37,8°C or/and cough or sore throat). Then, a nasal swab will be performed in order to identified the influenza virus.
5 days maximum
Study Arms (1)
Influenza-like illness group
Interventions
An interview to collect some informations will be done: demographic informations, medical history, vaccination against influenza status, symptoms and virological informations. Then, a nasal swab was performed in order to identified the influenza virus.
Eligibility Criteria
Each patient or health-care worker who present ILI (influenza-like illness) at admission or during hospitalization. ILI is defined by fever \> 37,8°C or/and cough or sore throat.
You may qualify if:
- Adult patients and health-care workers in a participating unit in the study,
- more than 18 years old,
- volunteers,
- who present an influenza-like illness defined by fever \> 37,8°C or/and cough or sore throat.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Infection Control unit. Edouard Herriot hospital Lyon - France
Lyon, 69003, France
Biospecimen
nasal swab
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 22, 2018
First Posted
January 29, 2018
Study Start
February 1, 2018
Primary Completion
June 1, 2018
Study Completion
June 1, 2022
Last Updated
January 30, 2018
Record last verified: 2018-01
Data Sharing
- IPD Sharing
- Will not share