- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03679416
Is There a Benefit of Whole Body Computed Tomography (WBCT) for Patients With Only High Velocity Road Traffic Collision (RTC) Vittel Criteria? (Cinescan)
For victims of high velocity RTC, with no other Vittel criteria of gravity, normal clinical examination of the thorax, abdomen and pelvis and Glasgow Coma Scale (GCS) score of 15 :
- Study of clinically unsuspected injuries discovered on WBCT
- Description
- Predictive factors
- Diagnostic performances of kinetic elements of Vittel criteria, and results of examinations realised at the ED.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Rennes, France, 35033
- Centre Hospitalier Universitaire de Rennes
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Consecutives patients consulting the emergency department between August 1st 2016 and July 31th 2017 :
- Older than 18 y.o.
- WBCT performed,
- Victim of a high velocity RTC as defined by the presence of at least one criteria of the kinetics elements of the Vittel Criteria
- Normal physical exam of the chest, abdomen and pelvis,
- GCS score of 15
Exclusion Criteria:
- Opposition of the patient to the use of their CT-scan for research
- Patients who are under legal protection
- Patients who are incarcerated
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of injuries diagnosed by Whole Body Computed Tomography (WBCT) that were not clinically suspected.
Time Frame: The day of inclusion
|
Number of injuries diagnosed by WBCT that were not clinically suspected. Classification in 3 categories according to their management :
|
The day of inclusion
|
Collaborators and Investigators
Sponsor
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
Other Study ID Numbers
- 35RC17-3082_Cinescan
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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