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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04778332
Other study ID # Trottinette19-20
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2019
Est. completion date March 31, 2021

Study information

Verified date April 2022
Source Centre Hospitalier Universitaire Saint Pierre
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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.


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 .


Recruitment information / eligibility

Status Completed
Enrollment 170
Est. completion date March 31, 2021
Est. primary completion date June 30, 2020
Accepts healthy volunteers No
Gender All
Age group 16 Years and older
Eligibility 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 Design


Locations

Country Name City State
Belgium CHU saint-Pierre Bruxelles

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire Saint Pierre

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary description of traumatic injuries description of traumatic injuries based on the medical record. Categorised by severity and by anatomical localisation. during the first 24 hours.
Primary Arrival mode By ambulance or by own means Up to one year
Primary Timing of arrival Immediately after the accident or delayed visit. Baseline
Primary Accident mechanism Other party ( Pedestrians hit by the scooter, accident with another) involved or not ( Loss of balance,2 drivers on the e-scooter, Baseline
Primary alcohol Did the driver report to being under the influence of alcohol or not baseline up to 24 hours
Primary Hour of admission Admission between 7am-6pm; 6pm-11pm or 11pm-7am Baseline up to 24 hours
Primary Ownership E-scooter owned or rented by the patient Baseline up to 24 hours
Secondary Treatment Emergency department or operative room Up to 24 hours
Secondary Paraclinical examination radiography, scanner, Up to 24 hours
Secondary orientation Intensive care unit, normal hospitalisation, discharge home Up to 24 hours
Secondary Cost of the treatment Ambulance, hospitalisation, treatment in the ED or operative room , temporary incapacity for work. Through study completion, an average of 1 year
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