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.
Studienübersicht
Status
Detaillierte Beschreibung
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 .
Studientyp
Einschreibung (Tatsächlich)
Kontakte und Standorte
Studienorte
-
-
-
Bruxelles, Belgien, 1000
- CHU Saint-Pierre
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Probenahmeverfahren
Studienpopulation
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
description of traumatic injuries
Zeitfenster: during the first 24 hours.
|
description of traumatic injuries based on the medical record.
Categorised by severity and by anatomical localisation.
|
during the first 24 hours.
|
|
Arrival mode
Zeitfenster: Up to one year
|
By ambulance or by own means
|
Up to one year
|
|
Timing of arrival
Zeitfenster: Baseline
|
Immediately after the accident or delayed visit.
|
Baseline
|
|
Accident mechanism
Zeitfenster: Baseline
|
Other party ( Pedestrians hit by the scooter, accident with another) involved or not ( Loss of balance,2 drivers on the e-scooter,
|
Baseline
|
|
alcohol
Zeitfenster: baseline up to 24 hours
|
Did the driver report to being under the influence of alcohol or not
|
baseline up to 24 hours
|
|
Hour of admission
Zeitfenster: Baseline up to 24 hours
|
Admission between 7am-6pm; 6pm-11pm or 11pm-7am
|
Baseline up to 24 hours
|
|
Ownership
Zeitfenster: Baseline up to 24 hours
|
E-scooter owned or rented by the patient
|
Baseline up to 24 hours
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Treatment
Zeitfenster: Up to 24 hours
|
Emergency department or operative room
|
Up to 24 hours
|
|
Paraclinical examination
Zeitfenster: Up to 24 hours
|
radiography, scanner,
|
Up to 24 hours
|
|
orientation
Zeitfenster: Up to 24 hours
|
Intensive care unit, normal hospitalisation, discharge home
|
Up to 24 hours
|
|
Cost of the treatment
Zeitfenster: Through study completion, an average of 1 year
|
Ambulance, hospitalisation, treatment in the ED or operative room , temporary incapacity for work.
|
Through study completion, an average of 1 year
|
Mitarbeiter und Ermittler
Ermittler
- Hauptermittler: Pierre YOUATOU TOWO, Centre Hospitalier Universitaire Saint Pierre
Publikationen und hilfreiche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- Trottinette19-20
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
IPD-Sharing-Zeitrahmen
IPD-Sharing-Zugriffskriterien
Art der unterstützenden IPD-Freigabeinformationen
- STUDIENPROTOKOLL
- SAFT
- ANALYTIC_CODE
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur Alkohol trinken
-
HBSARekrutierungBinge Drinking, Alkoholkonsum Minderjähriger, Trinken und Autofahren, alkoholbedingte SchädenVereinigte Staaten