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CompletedNCT05404425NIEPCEUpdated Nov 18, 2023

Non-severe Traumatic Injuries Evaluation Using smartPhone Camera for Extra-hospital Regulation

An interventional study of Visioconference: live visual injury evaluation and Control in Mild Traumatic Injury, Pre-hospital Dispatching and Visioconference, sponsored by Poitiers University Hospital. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-11-18.

Sponsored by Poitiers University Hospital · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
168
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Photography teletransmission allow a better and optimized dispatching of patients calling an Emergency Medical Call Center (EMCC) for a mild traumatic injury. It has previously been studied for patients to whom an ambulance was sent and therefore presumed to be older or with co-morbidities. The present trial aim to evaluate in the general population, the effect of a smartphone-mediated visioconference in the dispatching of patients calling an EMCC for mild traumatic injury.

02

Conditions studied

  • Mild Traumatic Injury
  • Pre-hospital Dispatching
  • Visioconference

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03

In context

Wounds and Injuries

5,056 studies on the registry are indexed under Wounds and Injuries; 861 are open to participants now.

This study's enrollment of 168 is above the median of 52 across 3,239 interventional studies indexed under Wounds and Injuries.

Browse Wounds and Injuries studies →

Lead sponsor

Poitiers University Hospital is the lead sponsor of 310 studies on the registry; 64 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

Inclusion criteria

  • adult patients (≥18 years of age),
  • free of will (not under any guardianship or liberty privation),
  • suffering from Mild Traumatic Injury,
  • availability of a smartphone with internet connection for the patients or witness,
  • consenting to participate in the study

Exclusion criteria

Exclusion Criteria:

  • severe trauma requiring immediate medical assistance
  • trauma associated with head injury, on antiplatelet therapy (APT) or anti-coagulation therapy (ACT)
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
168 participants (actual)

Study arms

  • Experimental
    Visioconference: live visual injury evaluation

    For patients randomized in the intervention group, a live visual evaluation of the injury is performed by the Emergency Medical Call Center physician using a dedicated, secure smartphone app

    Procedure: Visioconference: live visual injury evaluation

  • Other
    Standard Procedure

    Usual management of patients

    Procedure: Control

Interventions

  • ProcedureVisioconference: live visual injury evaluation

    For patients randomized in the intervention group, a live visual evaluation of the injury is performed by the Emergency Medical Call Center physician using a dedicated, secure smartphone app

  • ProcedureControl

    For patients randomized in the control group, the evaluation is performed by the Emergency Medical Call Center physician only by pone call

06

What researchers measure

Primary outcomes

  1. Proportion of patients dispatched elsewhere than to the nearest hospital

    Proportion of patients dispatched elsewhere than to the nearest hospital (left at home for outpatient care / referred to a higher-level hospital / handled by MICA for advanced pre-hospital medical care)

    Time frame: 1 year

Secondary outcomes

  1. Under-triage

    Under-triage : the proportion of patients initially left at home for outpatient care who had to visit an ED within the 10 following days for care related to the initial traumatic injury

    Time frame: 1 year

  2. Over-triage

    Over-triage : the proportion of patients initially dispatched to an ED who could have underwent outpatient care

    Time frame: 1 year

07

Study locations

1 site
  • Chu of Poitiers
    Poitiers, 86021, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 18, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05404425
Lead sponsor
Poitiers University Hospital
Responsible party
Sponsor
First posted
Jun 3, 2022
Start date
Jul 8, 2022
Primary completion
Oct 19, 2023
Completion
Oct 30, 2023
Last update
Nov 18, 2023

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2023. You cannot join it, but the record below documents what was studied.

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