Predictive Tracking of Patient Flow in the Emergency Services During the Virus Winter Epidemics
NCT ID: NCT02858531
Last Updated: 2024-03-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
760000 participants
OBSERVATIONAL
2016-09-01
2023-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Development and Validation of a Regional Multi-scale System for the Prediction of the Patient Flow in the Emergencies and the Need for Hospitalization
NCT03051737
Prognosis of Geriatric Patients With Non-bedded Night in the Emergency Department: a Multicenter Cohort Study
NCT05821491
Reorientation of Tripped Patients 4 and 5 in Emergency Department
NCT05392829
Prediction of Emergency Department Admission Volume
NCT07013825
Evaluation of the COVID-19 Infection Response in Patients Admitted to the Emergency Department for Dyspnea
NCT04422587
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
patients < 24 months or 60 years with bronchiolitis or ARF
ARF = Acute Renal Failure
data retrieval
data retrieval with the Hospital Information System
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
data retrieval
data retrieval with the Hospital Information System
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* elderly \< 60 years with acute renal failure or breathing problem
Exclusion Criteria
1 Month
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Centre Hospitalier Universitaire de Saint Etienne
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Olivier MORY, MD
Role: PRINCIPAL_INVESTIGATOR
Centre Hospitalier Universitaire de Saint Etienne
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
CHU de Grenoble (adult emergency service)
Grenoble, , France
CHU de Grenoble (pediatric service)
Grenoble, , France
CHU de Lyon (adult emergency service)
Lyon, , France
CHU de Lyon (laboratory of virology)
Lyon, , France
CHU de Lyon HFME (pediatric service)
Lyon, , France
CHU de Saint Etienne (adult emergency service)
Saint-Etienne, , France
CHU de Saint Etienne (Pediatric service)
Saint-Etienne, , France
CH de Valence (adult emergency service)
Valence, , France
CH de Valence (pediatric service)
Valence, , France
CH de Villefranche (adult emergency service)
Villefranche-sur-Saône, , France
CH de Villefranche (pediatric service)
Villefranche-sur-Saône, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
1969303 v 0
Identifier Type: OTHER
Identifier Source: secondary_id
1508191
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.