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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05404425
Acronym
NIEPCE
Enrollment
168
Registered
2022-06-03
Start date
2022-07-08
Completion date
2023-10-30
Last updated
2023-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mild Traumatic Injury, Pre-hospital Dispatching, Visioconference

Brief 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.

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

Sponsors

Poitiers University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

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

Design outcomes

Primary

MeasureTime frameDescription
Proportion of patients dispatched elsewhere than to the nearest hospital1 yearProportion 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)

Secondary

MeasureTime frameDescription
Under-triage1 yearUnder-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
Over-triage1 yearOver-triage : the proportion of patients initially dispatched to an ED who could have underwent outpatient care

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026