- ICH GCP
- US Clinical Trials Registry
- Clinical Trial 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.
Study Overview
Status
Detailed Description
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 .
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Bruxelles, Belgium, 1000
- CHU Saint-Pierre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
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
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
description of traumatic injuries
Time Frame: 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
Time Frame: Up to one year
|
By ambulance or by own means
|
Up to one year
|
Timing of arrival
Time Frame: Baseline
|
Immediately after the accident or delayed visit.
|
Baseline
|
Accident mechanism
Time Frame: 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
Time Frame: 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
Time Frame: Baseline up to 24 hours
|
Admission between 7am-6pm; 6pm-11pm or 11pm-7am
|
Baseline up to 24 hours
|
Ownership
Time Frame: Baseline up to 24 hours
|
E-scooter owned or rented by the patient
|
Baseline up to 24 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Treatment
Time Frame: Up to 24 hours
|
Emergency department or operative room
|
Up to 24 hours
|
Paraclinical examination
Time Frame: Up to 24 hours
|
radiography, scanner,
|
Up to 24 hours
|
orientation
Time Frame: Up to 24 hours
|
Intensive care unit, normal hospitalisation, discharge home
|
Up to 24 hours
|
Cost of the treatment
Time Frame: 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
|
Collaborators and Investigators
Investigators
- Principal Investigator: Pierre YOUATOU TOWO, Centre Hospitalier Universitaire Saint Pierre
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Trottinette19-20
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ANALYTIC_CODE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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