Emergency Department PatientRIGHT BEDNCT07347847
Impact on Mortality of Hospitalisation of a Patient in a Hospital Bed That Does Not Correspond to His Needs After a Visit to the Emergency Department
An observational study of Emergency Department Patient, run by Rennes University Hospital at 7 sites in France.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Emergency Department Patient
- How many people
- 2,766 participants
- Where
- 7 sitesFrance
- Study dates
- Jan 2026to Sep 2026
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: - People Presenting at an emergency department
Who may be able to join
- Presenting at an emergency department participating in the study,
- Requiring hospitalisation
Who cannot join
- Patients hospitalised in short-stay units with secondary outpatient care,
- Adults subject to legal protection (legal guardianship, curatorship, trusteeship), persons deprived of their liberty.
Trial locations and contacts
7 sites in 1 country. Contact the study team or a site near you to ask about taking part.
7 sites in 1 country
France7 sites
CHU Angers
Angers
Delphine DOUILLET, +33241353637, delphine.douillet@chu-angers.fr
Delphine Douillet
CH Le Mans
Le Mans
Lionel Imsaad, +332 43 43 43 43, limsaad@ch-lemans.fr
Lionel Imsaad
CHU Nantes
Nantes
Emmanuel Montassier, +332 40 08 33 33, Emmanuel.MONTASSIER@chu-nantes.fr
Emmanuel Montassier
CHU Poitiers
Poitiers
Nicolas Marjanovic, +330549444444, nicolas.marjanovic@chu-poitiers.fr
Nicolas Marjanovic
CHU Strasbourg
Strasbourg
Pierrick Le Borgne, +333 88 11 67 68, pierrick_med@yahoo.fr
Pierrick Le Borgne
CHU Toulouse
Toulouse
Margaux Piechowiak, +335 61 77 22 33, Piechowiak.m@chu-toulouse.fr
Margaux Piechowiak
CHU Tours
Tours
Geoffroy Rousseau, +332.47.47.47.47, geoffroy.rousseau@chu-tours.fr
Geoffroy Rousseau
About this study
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.
- Conditions
- Emergency Department Patient
- Being tested
- No intervention
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
No interventionOther
no intervention
What is being measured
The primary outcome is the main question the study is designed to answer.
Death rate
Measured: 30 days
Secondary outcomes (3)
Duration of hospitalization
Measured: 30 days
length of stay in the emergency department
Measured: 30 days
Rate of Adverse events
Adverse events occuring during hospitalization
Measured: 30 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Jan 2026
- Study startJan 2026 (estimated)
- Primary completionSep 2026 (estimated)
- Study completionSep 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Emergency Department PatientStudies of the same condition, open and under way.
- More trials run by Rennes University HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 2,766 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Rennes University Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- François Saget, Study chair, francois.saget@chu-rennes.fr
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07347847
- Sponsor's protocol ID
- 35RC25_30013
- Acronym
- RIGHT BED
- Status last verified
- Jan 2026
- First submitted
- 8 Jan 2026
- Last updated
- 21 Jan 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 21 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Impact on Mortality of Hospitalisation of a Patient in a Hospital Bed That Does Not Correspond to His Needs After a Visit to the Emergency Department
- ClinicalTrials.gov ID
- NCT07347847
- Acronym / sponsor ID
- RIGHT BED / 35RC25_30013
- Conditions
- Emergency Department Patient
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 2,766 participants (estimated)
- Lead sponsor
- Rennes University HospitalUniversity, hospital or other
- Study start
- Jan 2026 (estimated)
- Primary completion
- Sep 2026 (estimated)
- Study completion
- Sep 2026 (estimated)
- First posted
- 16 Jan 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- - People Presenting at an emergency department
Key inclusion criteria (2 listed)
- Presenting at an emergency department participating in the study,
- Requiring hospitalisation
Key exclusion criteria (2 listed)
- Patients hospitalised in short-stay units with secondary outpatient care,
- Adults subject to legal protection (legal guardianship, curatorship, trusteeship), persons deprived of their liberty.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| No interventionno intervention | Other | – |
Primary outcome
Death rate
Time frame: 30 days
3 secondary outcomes
Duration of hospitalization
Time frame: 30 days
length of stay in the emergency department
Time frame: 30 days
Rate of Adverse events
Time frame: 30 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Jan 2026.
Related trials for Emergency Department Patient
Recruiting
Development and Preliminary Validation of Intelligent Video Laryngoscope for Emergency Use
Critically Ill Patients Requiring Mechanical Ventilation
Recruiting
The Impact of Telemedicine, Using the Caller's Mobile Phone Camera, on the Quality of Care Provided to Adult Patients Contacting the 15 Centre for Acute Dyspnea
Dyspnea
Recruiting
WIN Ratio Analysis to Determine a Strategy of Non- Invasive SUpport for Respiratory Failure in the EmeRgency Department
Acute Hypoxic Respiratory Failure, Acute Respiratory Distress Syndrome (ARDS)
Recruiting
The Impact of MeMed BV® on Management of Patients With Suspected Lower Respiratory Tract Infections (LRTI) in the Emergency Department (ED) and Urgent Care Center (UCC) ("JUPITER" TRIAL)
Lower Respiratory Tract Infection
Recruiting
Peer Support Workers Study
Substance Use Disorder (SUD)
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
François Saget study chair
francois.saget@chu-rennes.fr
7 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Emergency Department Patient, run by Rennes University Hospital at 7 sites in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 21 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 7 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact François Saget, Md (+33299284321, francois.saget@chu-rennes.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Death rate (time frame: 30 days). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Jan 2026.