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Not yet recruitingNCT07929168BODY91Updated Nov 10, 2026

Analysis of the Positivity Rate of Sector-based Whole-body CT Scans in Grade C Trauma Patients in Essonne

An observational study in Multiple Trauma/Injuries and Wounds and Injuries, sponsored by Centre Hospitalier Sud Francilien. Not yet recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by Centre Hospitalier Sud Francilien · Observational

Updated Nov 10, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
100
Ages
18 Years and older
Sex
All
01

Study summary

Background: Grade C trauma patients show no obvious severe injury at first assessment, but the mechanism or circumstances of the accident make serious lesions possible. Guidelines recommend a whole-body CT scan as first-line imaging1. The organization of the French trauma system varies between regions2. Île-de-France distinguishes level 1 trauma centers, which are authorized to manage the most severe patients, from level 2 hospitals, which can perform a full injury assessment3. Essonne has no level 1 trauma center, and most are located in Paris. Emergency dispatch physicians must therefore choose between performing the scan at the local hospital or transporting the patient directly to a trauma center. When a local scan is abnormal, specialist consultation, image transfer and secondary transport take time (median of about 6 hours4) and may worsen the prognosis.

Objective: To assess whether the proportion of abnormal whole-body CT scans in grade C trauma patients justifies systematic transport to a trauma center rather than local imaging.

Methods: Retrospective, multicenter cohort study of about 100 adult grade C trauma patients managed by an Essonne mobile emergency team (SMUR) in 2025 who underwent a whole-body CT scan. We will determine the proportion of abnormal scans, whether the lesions could be managed locally or required a level 1 or 2 trauma center, the secondary transfer rate, and the time to final destination.

Hypothesis: The proportion of abnormal scans, particularly those requiring specific medical care, is high enough to support performing the first whole-body CT scan at a trauma center.

Read the detailed description

Grade C trauma patients are a diagnostic and logistical challenge: their initial presentation is reassuring, yet the mechanism of injury may conceal severe lesions, which is why whole-body CT is recommended as first-line imaging6. The destination chosen at the pre-hospital stage therefore determines both the speed of diagnosis and the speed of access to specialized care. In Essonne, where no level 1 trauma center exists, this choice is made by the SAMU dispatch physician, case by case, without local data on how often a scan performed at the sector hospital reveals lesions requiring specialized management. The delays reported after an abnormal local scan are the main argument for direct transfer, while the unnecessary mobilization of resources and the transport of patients who turn out to have normal scans are the main argument against.

This is a retrospective, multicenter, observational cohort study. It covers hospitals of the Essonne department that received grade C trauma patients managed by an Essonne SMUR team in 2025 and who received a whole-body CT. Cases will be identified from SMUR and SAMU activity records, then linked to the receiving hospitals' medical files. No intervention will be performed and no change to patient care is planned.

Data will be extracted from SAMU dispatch records, emergency department files and radiology reports. Variables will include:

  • demographics and relevant medical history
  • mechanism of injury and pre-hospital clinical findings
  • time stamps for each care step (SMUR arrival on scene, hospital arrival, scan, specialist consultation, secondary transport, arrival at final destination)
  • whole-body CT findings
  • the level of care needed (local hospital, level 2 or level 1 trauma center)
  • secondary transfers, and the regulation time required for them

Data will be recorded in a pseudonymized, secure database. Descriptive statistics will be used for the whole cohort. The proportion of abnormal whole-body CT scans will be reported with its 95% confidence interval.

02

Conditions studied

  • Multiple Trauma/Injuries
  • Wounds and Injuries

Keywords

  • Whole-body computed tomography
  • Tomography
  • Whole Body Imaging
  • Multiple Trauma
  • Trauma Centers
  • Emergency Medical Services
  • Prehospital emergency care
  • Retrospective Studies
03

In context

Multiple Trauma

139 studies on the registry are indexed under Multiple Trauma; 32 are open to participants now.

This study's planned enrollment of 100 is below the median of 200 across 84 observational studies indexed under Multiple Trauma.

Browse Multiple Trauma studies →

Lead sponsor

Centre Hospitalier Sud Francilien is the lead sponsor of 58 studies on the registry; 13 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult grade C trauma patients attended on scene by a mobile emergency and resuscitation team (SMUR) of Essonne between 01/01/2024 and 31/12/2025, who underwent a whole-body CT scan at the sector hospital. Grade C patients are stable at first assessment, with no obvious severe injury, but their mechanism of injury and/or medical background make severe lesions possible. Patients are identified from the Essonne SAMU dispatch software and from the medical records of the emergency departments of the participating hospitals.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age over 18 years
  • Grade C trauma patient managed between 01/01/2025 and 31/12/2025
  • Having undergone a whole-body CT scan
  • Attended by an Essonne SMUR team

Exclusion criteria

Exclusion Criteria:

  • Trauma patient meeting grade A or B criteria
  • Low-kinetic accident and/or patient without an at-risk medical background
  • No on-scene SMUR intervention
  • Refusal of transport
  • Taken to a level 1 trauma center as destination
  • Patient who objected to the use of their data
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Line of therapy

A line of therapy is one course of treatment, which may combine several drugs. First-line is the first course given; second-line follows when that stops working or is not tolerated.

“Two prior lines” means two courses that count separately under the study’s rules — not simply two drugs. Ask the study team if you are unsure how yours are counted.

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • Grade C trauma patients with sector whole-body CT

    Adult (\>18 years) grade C trauma patients attended on scene by an Essonne SMUR team between 01/01/2025 and 31/12/2025, who underwent a whole-body CT scan at the sector hospital. A grade C patient is stable (no hemodynamic disorder) and meets no grade A or B criterion, but has a high-risk mechanism of injury (fall of more than 6 m, ejected, crushed, thrown or blasted victim, death of a passenger in the same vehicle, proximal open limb fracture or closed fracture of at least 2 long bones) and/or an at-risk medical background.

    Diagnostic Test: Whole-body CT scan at the sector hospital

Interventions

  • Diagnostic testWhole-body CT scan at the sector hospital

    Whole-body computed tomography performed as first-line imaging in the radiology department of the sector hospital covering the accident site, as part of routine care. Its results (trauma-related lesions, level of care required, secondary transfer to a trauma center) are analysed retrospectively.

06

What researchers measure

Primary outcomes

  1. Proportion of pathological whole-body CT scans

    A whole-body CT scan is considered pathological if it shows trauma-related lesions on imaging, whatever their severity. Lesions discovered incidentally or present before the accident are not counted. Data are collected from the Essonne SAMU dispatch software and, for missing data, by calling the receiving emergency departments of the sector hospitals.

    Time frame: at day 0

Secondary outcomes

  1. Rate of secondary transfers to a trauma center

    Final orientation of patients with a pathological whole-body CT scan, analysed qualitatively: proportion of patients secondarily transferred to a level 1 trauma center or an intensive care unit, and distribution between patients who can be managed at the sector hospital and those requiring care in a level 1 or level 2 trauma center.

    Time frame: at day 0

  2. Total time from initial SMUR care to arrival at the final destination

    Total duration between the initial SMUR care and the arrival of the patient at the final destination, used to evaluate the impact of under-triage of grade C trauma patients by comparison of delays (Wilcoxon test). Delays are described as medians with interquartile ranges.

    Time frame: at day 0

  3. Proportion of pathological whole-body CT scans according to the collected variables

    Descriptive analysis of the cohort of grade C trauma patients: proportion of pathological scans according to age, sex, medical background, type of accident and the criterion defining grade C.

    Time frame: at day 0

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Nov 2026; primary completion for Nov 2027, 12 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 5, 2026
First posted
Nov 10, 2026
StartEst.
Nov 15, 2026
Primary completionEst.
Nov 15, 2027
CompletionEst.
Nov 15, 2027
Last update
Nov 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 10, 2026
Show all 1 update
  1. Nov 10, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07929168
Lead sponsor
Centre Hospitalier Sud Francilien
Responsible party
Sponsor
First posted
Nov 10, 2026
Start date
Nov 15, 2026 (estimated)
Primary completion
Nov 15, 2027 (estimated)
Completion
Nov 15, 2027 (estimated)
Last update
Nov 10, 2026

Study contacts

Victor VIGER, MD
Contact
victor.viger@chsf.fr
1 61 13 95 56 ext. +33
Caroline TOURTE
Contact
caroline.tourte@chsf.fr
1 61 69 31 50 ext. +33

Oversight

Data monitoring committee
No
FDA-regulated drug
No
View the source record on ClinicalTrials.gov ↗

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