- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT04778332
Trottinettes Urgences 2019-2020
Risk Assessment, Consequences and Epidemiology of Electric Scooter Accidents Admitted to Emergency Departments.
The purpose of the study was to evaluate the risk, consequences and epidemiology of electric scooter accidents admitted to the emergency room at St. Pierre University Hospital.
This prospective observational study aims to include any patient admitted to the Adult Emergency Department of St.Pierre University Hospital Brussels following an accident related to the use of an electric scooter in order to describe and understand the epidemiology, complications and treatment of injuries associated with this means of transport.
It is intended to include all accidents occurring in the emergency room during the period from 01/06/2019 to 30/06/2020.
Studieöversikt
Status
Detaljerad beskrivning
All patients over the age of 16 years with traumatic injuries due to an accident related to the use of an electric scooter were included in the study.
Upon admission to the Emergency Department, patients over 16 years of age who accepted were included in the study. The objectives of the study were firstly to describe the context and incidence of scooter accidents, and secondly to understand the epidemiology, complications and treatment of injuries associated with this means of transport and finally, to estimate the economic impact assessed by the number of days of post-traumatic work disability, the need for access to more specialised and therefore more expensive care (operating theatre interventions, scanner-type radiological examinations or hospitalisation in intensive care units).
The data analyzed were based on :
1) the time and day of the accident, 2) the time of presentation at the hospital (same day or after the accident), 3) the mechanism of the accident, whether there were one or two people on the scooter, 4) the use or non-use of the protective helmet, 5) the influence of alcohol ; 6) the mode of arrival at the emergency room (type of ambulance or by one's own means); 7) the injury assessment, paraclinical examinations; 8) treatments; 9) hospitalization or not; 10) temporary work interruptions .
Studietyp
Inskrivning (Faktisk)
Kontakter och platser
Studieorter
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-
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Bruxelles, Belgien, 1000
- CHU Saint-Pierre
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Testmetod
Studera befolkning
Beskrivning
Inclusion criteria:
- All patients with traumatic lesion following electric sccoter accident
- Be able to agree to participate in the study
Exclusion Criteria:
- < 16 years
- Unconscious
- Being unable to agree to participate in the study
Studieplan
Hur är studien utformad?
Designdetaljer
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
description of traumatic injuries
Tidsram: during the first 24 hours.
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description of traumatic injuries based on the medical record.
Categorised by severity and by anatomical localisation.
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during the first 24 hours.
|
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Arrival mode
Tidsram: Up to one year
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By ambulance or by own means
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Up to one year
|
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Timing of arrival
Tidsram: Baseline
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Immediately after the accident or delayed visit.
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Baseline
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Accident mechanism
Tidsram: Baseline
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Other party ( Pedestrians hit by the scooter, accident with another) involved or not ( Loss of balance,2 drivers on the e-scooter,
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Baseline
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alcohol
Tidsram: baseline up to 24 hours
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Did the driver report to being under the influence of alcohol or not
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baseline up to 24 hours
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Hour of admission
Tidsram: Baseline up to 24 hours
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Admission between 7am-6pm; 6pm-11pm or 11pm-7am
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Baseline up to 24 hours
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Ownership
Tidsram: Baseline up to 24 hours
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E-scooter owned or rented by the patient
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Baseline up to 24 hours
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Treatment
Tidsram: Up to 24 hours
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Emergency department or operative room
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Up to 24 hours
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Paraclinical examination
Tidsram: Up to 24 hours
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radiography, scanner,
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Up to 24 hours
|
|
orientation
Tidsram: Up to 24 hours
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Intensive care unit, normal hospitalisation, discharge home
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Up to 24 hours
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Cost of the treatment
Tidsram: Through study completion, an average of 1 year
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Ambulance, hospitalisation, treatment in the ED or operative room , temporary incapacity for work.
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Through study completion, an average of 1 year
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Samarbetspartners och utredare
Utredare
- Huvudutredare: Pierre YOUATOU TOWO, Centre Hospitalier Universitaire Saint Pierre
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- Trottinette19-20
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
IPD-planbeskrivning
Tidsram för IPD-delning
Kriterier för IPD Sharing Access
IPD-delning som stöder informationstyp
- STUDY_PROTOCOL
- SAV
- ANALYTIC_CODE
Läkemedels- och apparatinformation, studiedokument
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