- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg 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.
Studieoversigt
Status
Detaljeret beskrivelse
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 .
Undersøgelsestype
Tilmelding (Faktiske)
Kontakter og lokationer
Studiesteder
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Bruxelles, Belgien, 1000
- CHU Saint-Pierre
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
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
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
description of traumatic injuries
Tidsramme: 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
Tidsramme: 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
Tidsramme: Baseline
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Immediately after the accident or delayed visit.
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Baseline
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Accident mechanism
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Treatment
Tidsramme: 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
Tidsramme: Up to 24 hours
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radiography, scanner,
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Up to 24 hours
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orientation
Tidsramme: 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
Tidsramme: 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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Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Pierre YOUATOU TOWO, Centre Hospitalier Universitaire Saint Pierre
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- Trottinette19-20
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
IPD-delingstidsramme
IPD-delingsadgangskriterier
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
- SAP
- ANALYTIC_CODE
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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