Comparing Use of a Prehospital Ultrasound System and Standard Prehospital Care in Thoracoabdominal Trauma
NCT ID: NCT02198885
Last Updated: 2017-11-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
12 participants
OBSERVATIONAL
2014-08-31
2017-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Control
This group receives the standard prehospital care en route to hospital, and they do not receive the FAST ultrasound en route.
No interventions assigned to this group
FAST
This group receives the FAST ultrasound en route to hospital.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patient presenting with blunt or penetrating trauma to the thorax or abdomen
* Patient transported by MD Ambulance to Royal University Hospital
* Patient being transported by a paramedic who has received training in the above ultrasound system and who has with them a NanoMaxx Ultrasound System (SonoSite) to be used in connection with the RP-Xpress (InTouch Technologies)
* Patient will take longer than 10 minutes to transport to hospital
* Patient's care will not be compromised in completing a FAST exam - opinion of paramedic
* Patient's care will not be compromised in completing a FAST exam - opinion of ER physician
* Patient is 18 years of age or older
* Patient presenting with blunt or penetrating trauma to the thorax or abdomen
* Patient transported by MD Ambulance to Royal University Hospital
* Patient will take longer than 10 minutes to transport to hospital
Exclusion Criteria
* Patients whose care would be compromised if other procedures of higher priority (as determined by paramedics and/or remotely-present physicians) were not be able to be executed due to time involved in completing a FAST exam
* Patients who are not being transported to Royal University Hospital
* Patients whose expected transport time from scene to hospital is less than 10 minutes
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Saskatoon Health Region
OTHER
M.D. Ambulance Care Ltd.
UNKNOWN
University of Saskatchewan
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ivar Mendez
M.D.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Ivar Mendez
Role: PRINCIPAL_INVESTIGATOR
University of Saskatchewan
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Royal University Hospital
Saskatoon, Saskatchewan, Canada
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Bio# 14-109
Identifier Type: OTHER
Identifier Source: secondary_id
FAST-01
Identifier Type: -
Identifier Source: org_study_id