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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03051737
Other study ID # NI15018
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 1, 2021
Est. completion date December 2023

Study information

Verified date March 2022
Source Assistance Publique - Hôpitaux de Paris
Contact Mathias WARGON, MD
Phone +33 1 49 83 10 86
Email m.wargon@ch-bry.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main objective of this retrospective study is to validate a prediction system of emergencies department (ED) attendance on a wide range of time and the need for hospitalization, at various levels of perimeter (with all emergency departments or one ED in particular), with all patients or with one sub-group of patients (age, gravity, care).


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.)


Recruitment information / eligibility

Status Recruiting
Enrollment 18000000
Est. completion date December 2023
Est. primary completion date December 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - All subjects have been recorded as patients in emergency departments between 2010 and 2015. Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Emergency Department - Bry sur Marne Hospital Bry sur Marne Val-de-Marne

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prediction of emergency department visits 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 Prediction by age By sub-group of child or senior throughout the study, an average of 18 months
Secondary Prediction by lever of gravity throughout the study, an average of 18 months
Secondary Prediction by type of care By type : (medical, surgical or intensive) care throughout the study, an average of 18 months
Secondary Prediction by need of hospitalization or no throughout the study, an average of 18 months
Secondary Relation between flow of patients and indicator of tension of team throughout the study, an average of 18 months
Secondary Relation between flow of patients and time of ED visit throughout the study, an average of 18 months
Secondary Typology of ED of the region of Paris throughout the study, an average of 18 months
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