NCT07013825

Brief Summary

Retrospective cohort. Schedule emergency service overload periods on different terms, by hour or time slot over several days.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Apr 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2023

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 15, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 15, 2023

Completed
1.6 years until next milestone

First Submitted

Initial submission to the registry

June 2, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

June 10, 2025

Completed
Last Updated

June 10, 2025

Status Verified

May 1, 2025

Enrollment Period

7 months

First QC Date

June 2, 2025

Last Update Submit

June 2, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Rate of admissions to emergency rooms

    01/01/2022 - 31/12/2022

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study participants will be selected from a population of patients who meet specific inclusion and exclusion criteria. Specifically, the population will consist of individuals who: Are adult patients (i.e., not minors), Have not refused to be included in the study, as indicated in their medical records, Have not objected to the use of their medical data or explicitly refused to participate, Have had at least one consultation at the emergency department in the year prior to the study period. Thus, the study population will include adult patients with documented emergency department visits in the past year, who have not opted out of data use and have no recorded refusal to participate.

Minor patients Refusal of inclusion in a study explicitly stated in the medical record Objection to the use of data or refusal to participate No consultation at the emergency department in the year prior to the study

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

Study Sites (1)

France

Saint-Denis, France, 93200, France

Location

MeSH Terms

Conditions

Emergencies

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 2, 2025

First Posted

June 10, 2025

Study Start

April 1, 2023

Primary Completion

October 15, 2023

Study Completion

October 15, 2023

Last Updated

June 10, 2025

Record last verified: 2025-05

Locations