- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03051737
Development and Validation of a Regional Multi-scale System for the Prediction of the Patient Flow in the Emergencies and the Need for Hospitalization (PRED-URG)
Development and Validation of a Regional Multi-scale System in Ile-de-France for the Prediction of the Patient Flow in the Emergency Department and the Need for Hospitalization
Study Overview
Status
Conditions
Detailed Description
As secondary objectives, the study aims:
- to measure the influence of different factors as environmental or structural and to identify the modifiable factors, then to allow us to test by simulation, impact of various interventions (for example: opening of hospitals and reinforcement of ED teams) on arrival flows or regenerated tension inside ED teams.
- to study the relation between the flows (arrival patients, hospitalized patients) and the time of ED visit or the indicators of tension of ED team.
- Typology of ED in the region of Paris permitting afterward comparison the benchmarking type between similar structures.
This retrospective study will be performed on database: individual data in the region of Paris of summation of ED visits and data on the structures of health cares, as well as environmental data (principal given cares, weather, moves, circulations, pollution, strikes, vacations, etc.)
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Mathias WARGON, MD
- Phone Number: +33 1 49 83 10 86
- Email: m.wargon@ch-bry.org
Study Locations
-
-
Val-de-Marne
-
Bry sur Marne, Val-de-Marne, France, 94360
- Recruiting
- Emergency Department - Bry sur Marne Hospital
-
Contact:
- Mathias WARGON, MD
- Phone Number: +33 1 49 83 10 86
- Email: m.wargon@ch-bry.org
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Adults or children who have been recorded as patients in emergency departments between 2010 and 2015 are all eligibles with unlimited number of care.
85 Health Facilities in Ile de France who have emergency departments will participate the study.
Description
Inclusion Criteria:
- All subjects have been recorded as patients in emergency departments between 2010 and 2015.
Exclusion Criteria:
- None
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prediction of emergency department visits
Time Frame: throughout the study, an average of 18 months
|
Calculated base on regional database: individual data of summation of ED visits in the region of Paris and structural data of health cares
|
throughout the study, an average of 18 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prediction by age
Time Frame: throughout the study, an average of 18 months
|
By sub-group of child or senior
|
throughout the study, an average of 18 months
|
Prediction by lever of gravity
Time Frame: throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
|
Prediction by type of care
Time Frame: throughout the study, an average of 18 months
|
By type : (medical, surgical or intensive) care
|
throughout the study, an average of 18 months
|
Prediction by need of hospitalization or no
Time Frame: throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
|
Relation between flow of patients and indicator of tension of team
Time Frame: throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
|
Relation between flow of patients and time of ED visit
Time Frame: throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
|
Typology of ED of the region of Paris
Time Frame: throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Mathias WARGON, MD, Emergency Department - Bry sur Marne Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
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
Other Study ID Numbers
- NI15018
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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