NCT07347847

Brief Summary

The aim of this study is to assess the impact of hospitalisation outside the referral requested by the emergency doctor on the mortality of patients admitted to emergency departments.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
2,766

participants targeted

Target at P75+ for all trials

Timeline
4mo left

Started Jan 2026

Shorter than P25 for all trials

Geographic Reach
1 country

7 active sites

Status
not yet recruiting

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 Progress52%
Jan 2026Sep 2026

Study Start

First participant enrolled

January 1, 2026

Completed
7 days until next milestone

First Submitted

Initial submission to the registry

January 8, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 16, 2026

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2026

Last Updated

January 21, 2026

Status Verified

January 1, 2026

Enrollment Period

8 months

First QC Date

January 8, 2026

Last Update Submit

January 16, 2026

Conditions

Emergency Department Patient

Outcome Measures

Primary Outcomes (1)

  • Death rate

    30 days

Secondary Outcomes (3)

  • Duration of hospitalization

    30 days

  • length of stay in the emergency department

    30 days

  • Rate of Adverse events

    30 days

Interventions

No interventionOTHER

no intervention

Eligibility Criteria

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

\- People Presenting at an emergency department

You may qualify if:

  • Presenting at an emergency department participating in the study,
  • Requiring hospitalisation

You may not qualify if:

  • Patients hospitalised in short-stay units with secondary outpatient care,
  • Adults subject to legal protection (legal guardianship, curatorship, trusteeship), persons deprived of their liberty.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (7)

CHU Angers

Angers, France

Location

CH Le Mans

Le Mans, France

Location

CHU Nantes

Nantes, France

Location

CHU Poitiers

Poitiers, France

Location

CHU Strasbourg

Strasbourg, France

Location

CHU Toulouse

Toulouse, France

Location

CHU Tours

Tours, France

Location

Study Officials

  • François Saget

    francois.saget@chu-rennes.fr

    STUDY CHAIR

Central Study Contacts

François Saget, Md

CONTACT

+33299284321francois.saget@chu-rennes.fr

Study Design

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

Study Record Dates

First Submitted

January 8, 2026

First Posted

January 16, 2026

Study Start

January 1, 2026

Primary Completion (Estimated)

September 1, 2026

Study Completion (Estimated)

September 1, 2026

Last Updated

January 21, 2026

Record last verified: 2026-01

Locations

FR(7)