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NCT04665778 Clinical Trial

Prediction of the Patient Pathway in Emergency Room in an Exceptional Sanitary Situation

Covid19 Clinical Trial

— 3PU-SSE  

Official title:
Prediction of the Patient Pathway in Emergency Room in an Exceptional Sanitary Situation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04665778
Other study ID # PI2020_843_0055
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 4, 2020
Est. completion date March 1, 2021

Study information
Verified date July 2021
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The COVID-19 outbreak leads to optimize the pathway in emergency departments. The length of time spent in the Emergency Department is linked to the morbi-mortality and the risk of COVID-19 transmission. The Amiens-Picardy University Hospital has developed an application (3P-U) that optimizes patient flow. It identifies the need of hospitalization and problems on the care path. Patients are categorized in high risk or not high probabilty of hospitalization. The main goal of this project is to evaluate the impact on the patient flow of the 3P-U application. Early lookup of bed for high probability hospitalization should be linked to a reduced time of length. This study will compare the time of length between this both groups.

Recruitment information / eligibility
Status Completed
Enrollment 1516
Est. completion date March 1, 2021
Est. primary completion date March 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - every patient that consults in the Adult Emergency Department Exclusion Criteria: - patients directly transferred to Intensive Care Units

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• hospital bedroom booking
Patient in high risk of hospitalization group benefits a dedicated process to find and book a bedroom

Locations
Country Name City State
France CHU Amiens Amiens

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Variation of the length of stay between high probability of hospitalization group and not high risk of hospitalization group. Variation of the length of stay between high probability of hospitalization group and not high risk of hospitalization group. up to 3 months
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