- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02858531
Predictive Tracking of Patient Flow in the Emergency Services During the Virus Winter Epidemics (PREDAFLU)
Epidemics and infectious diseases in general, punctuate much of the activity of an emergency service. The impact of winter infections is particularly important to vulnerable populations such as infant during bronchiolitis epidemics and the elderly during seasonal influenza. Each year, these epidemic phenomena lead to disorganization of emergency services and healthcare teams by lack of anticipation and organizational measures in particular to manage the approval of emergency services for the most vulnerable populations requiring hospitalization.
For 2 years, the pediatric emergency department of St Etienne University Hospital has a decision support tool for the periods of winter epidemics. Through a retrospective analysis of Passages of Emergency summary, this tool provides an estimate of infants with bronchiolitis flow day to day, and the availability in real time of an abnormally high flow of patients to pediatric emergencies. These data can help to affirm that the epidemic begins in this hospital.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Contact
- Name: Olivier MORY, MD
- Phone Number: (0)4 77 82 81 34
- Email: olivier.mory@chu-st-etienne.fr
Study Contact Backup
- Name: Béatrice DEYGAS
- Phone Number: (0)4 77 12 76 55
- Email: beatrice.deygas@chu-st-etienne.fr
Study Locations
-
-
-
Grenoble, France, 38000
- CHU de Grenoble (adult emergency service)
-
Grenoble, France, 38000
- CHU de Grenoble (pediatric service)
-
Lyon, France, 69000
- CHU de Lyon (adult emergency service)
-
Lyon, France, 69000
- CHU de Lyon (laboratory of virology)
-
Lyon, France, 69000
- CHU de Lyon HFME (pediatric service)
-
Saint Etienne, France, 42055
- CHU de Saint Etienne (adult emergency service)
-
Saint Etienne, France, 42055
- CHU de Saint Etienne (Pediatric service)
-
Valence, France, 26000
- CH de Valence (adult emergency service)
-
Valence, France, 26000
- CH de Valence (pediatric service)
-
Villefranche Sur Saone, France, 69655
- CH de Villefranche (adult emergency service)
-
Villefranche Sur Saone, France, 69655
- CH de Villefranche (pediatric service)
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- child < 24 months with bronchiolitis
- elderly < 60 years with acute renal failure or breathing problem
Exclusion Criteria:
- refuse of transmission of their data
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
patients < 24 months or 60 years with bronchiolitis or ARF
ARF = Acute Renal Failure
|
data retrieval with the Hospital Information System
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
build a predictive tool
Time Frame: at inclusion
|
a tool with different levels of alerts of the influx of people aged to emergencies during winter epidemics. Variables in the model : activity database in emergency services, computer data, virology database and average length of stay. |
at inclusion
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Difference between the estimated date and the effective date of the activity peak on the average length of stay of patients in the hospital of Saint Etienne
Time Frame: at inclusion
|
at inclusion
|
Difference between the estimated date and the effective date of the activity peak on the average length of stay of patients in the other hospitals
Time Frame: at inclusion
|
at inclusion
|
Comparison virological databases with clinical diagnosis of patients
Time Frame: at inclusion
|
at inclusion
|
Percentage of elderly staying more than 10 hours in the emergency services.
Time Frame: at inclusion
|
at inclusion
|
Collaborators and Investigators
Investigators
- Principal Investigator: Olivier MORY, MD, Centre Hospitalier Universitaire de Saint Etienne
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathologic Processes
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Lung Diseases
- Kidney Diseases
- Urologic Diseases
- Disease Attributes
- Bronchial Diseases
- Renal Insufficiency
- Lung Diseases, Obstructive
- Bronchitis
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urogenital Diseases
- Male Urogenital Diseases
- Emergencies
- Acute Kidney Injury
- Bronchiolitis
Other Study ID Numbers
- 1508191
- 1969303 v 0 (Other Identifier: CNIL)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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