NCT07769645

Brief Summary

The number of emergency department visits is constantly increasing France. Over the past three decades, the figure has risen from 10 million to more than 20 million visits per year. This is often attributed to a shortage of available primary care physicians and patients' inability to obtain timely appointments, whether for general practice or specialist consultations. It should also be noted that following the COVID-19 pandemic, the resurgence in emergency department attendance has further strained services. An aging population is associated with more advanced chronic conditions that are prone to decompensation, as well as more frequent acute illnesses resulting from increasing age-related frailty. In France, the healthcare system encompasses 719 emergency departments, predominantly located in public healthcare institutions. Emergency departments manage medical, psychiatric, surgical, and traumatological emergencies in both children and adults. The current context is further characterized by a reduction in the number of available downstream inpatient beds nationwide, with an average decrease of approximately 1,390 beds per year between 2014 and 2023. These various factors contribute to high emergency department utilization rates and occupancy levels. Emergency department length of stay has been shown to impact in-hospital mortality, particularly among patients aged 75 and over, and also negatively affects patient experience as well as the mental health of healthcare workers. One of the key challenges is to identify ways of reducing emergency department length of stay in order to improve patient flow and thereby decrease occupancy rates. Better control of these factors may also reduce morbidity and mortality associated with overcrowded emergency departments, as well as mean inpatient length of stay. Emergency department length of stay depends on multiple factors, including waiting time before triage and placement, time to medical advice, time to blood sampling and imaging results when ordered, and time to specialist consultation when required. Additional delays may also arise from waiting for an inpatient bed to become available. All of these steps affect length of stay but are necessary to establish an accurate diagnosis and determine the appropriate disposition for each patient. Triage, using the FRENCH scale applied to patients in this study, may itself have an impact when performed rigorously, although blood tests have been shown to outperform algorithm-based triage in predicting short-term mortality. However, when unnecessary tests are performed through systematic blood sampling, emergency department length of stay is prolonged. In the study by Strada, which evaluated anticipated blood sampling for abdominal pain, chest pain, and non-traumatic bleeding, a benefit was identified only for chest pain. Another study, conducted on a small sample, found no influence of blood testing on emergency department length of stay. A further study evaluated point-of-care testing in the emergency department, which significantly reduced the time between test ordering and result availability, but demonstrated no impact on emergency department length of stay. At the emergency department of the Centre Hospitalier de Roubaix, an increase in admissions and time to first medical contact has been observed, and several protocols have already been implemented to improve length of stay. Since November 2024, a high-flow procedure has been introduced enabling anticipated blood sampling prior to the first medical contact. The primary objective of the study is to evaluate the impact of anticipated blood sampling on emergency department length of stay. Secondary objectives include the impact of anticipated blood sampling on length of stay according to patient disposition, and its impact on time to first medical contact.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
28,421

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2025

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

January 1, 2025

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 4, 2026

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

August 9, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

August 18, 2026

Completed
Last Updated

August 18, 2026

Status Verified

April 1, 2026

Enrollment Period

12 months

First QC Date

August 9, 2026

Last Update Submit

August 12, 2026

Conditions

Keywords

OvercrowdingEmergency DepartmentAnticipated Blood Samplingpropensity score

Outcome Measures

Primary Outcomes (1)

  • lenght of stay

    Delay between admission and discharge of emergency department

    From ED admission to ED discharge, assessed over a 12-month period (January 1 to December 31, 2025)

Secondary Outcomes (1)

  • Time to doctor

    From ED admission to ED discharge, assessed over a 12-month period (January 1 to December 31, 2025)

Other Outcomes (1)

  • Anticipated Blood Sampling

    From ED admission to ED discharge, assessed over a 12-month period (January 1 to December 31, 2025)

Study Arms (2)

No ABS

Patient who don't have anticipated blood sampling

Procedure: No Anticipated Blood Sampling

ABS

Patient who have anticipated blood sampling

Procedure: Anticipated blood sampling

Interventions

Blood sampling was considered as anticipated if it has been realized a least 103 minutes before medical advice.

ABS

If blood sampling was realized between 103 minutes before medical advice a medical advice or after.

No ABS

Eligibility Criteria

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

All patients admitted in ED between 01/01/2025and 12/31/2025 wha had blood sampling.

You may qualify if:

  • years and older
  • Blood sampling realized in ED

You may not qualify if:

  • Patients without triage
  • Patients without complaint
  • Patient's refusal

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Hospitalire de Roubaix

Roubaix, 59100, France

Location

MeSH Terms

Conditions

CrowdingEmergencies

Condition Hierarchy (Ancestors)

Spatial BehaviorBehaviorDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Rémy Diesnis, MD

    Centre Hospirtalier de Roubaix

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Target Duration
12 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Medical Doctor, Head of Research Unit

Study Record Dates

First Submitted

August 9, 2026

First Posted

August 18, 2026

Study Start

January 1, 2025

Primary Completion

December 31, 2025

Study Completion

April 4, 2026

Last Updated

August 18, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations